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1. Presence of glycerokinase in guinea pig mammary gland and the incorporation of glycerol into glycerides

Author

O.W. McBride and Edward D. Korn

Subjects
Biochemistry, QD415-436
Abstract

The presence of glycerokinase in homogenates of mammary tissue from lactating guinea pigs is demonstrated. It has been shown that α-glycerophosphate-C14 (chromatographically identified) is formed from glvcerol-1,3-C14 in the presence of homogenate. This reaction requires ATP and Mg++. Glycerol-C14 is incorporated into the glycerol moiety of glycerides via α-glycerophosphate. G1ucose-C14 can also serve as a source of glyceride glycerol.

Published
1964
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2. Uptake of free fatty acids and chylomicron glycerides by guinea pig mammary gland in pregnancy and lactation

Author

O.W. McBride and Edward D. Korn

Subjects
Biochemistry, QD415-436
Abstract

Mammary tissue of lactating guinea pigs was shown to take up both free fatty acids and chylomicron glycerides from plasma approximately twenty times more rapidly than mammary glands from midpregnant animals. The rates of removal of both forms of lipid by lactating mammary gland are comparable with those of liver. Free fatty acids cross the placental membrane and are rapidly taken up by fetuses at midpregnancy. There is no transfer of chylomicron glyceride across the placental membrane.

Published
1964
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3. Acceptors of fatty acid for glyceride synthesis in guinea pig mammary gland

Author

O.W. McBride and Edward D. Korn

Subjects
Biochemistry, QD415-436
Abstract

Glycerides are shown to be synthesized by two pathways in mammary tissue of lactating guinea pigs. One pathway involves the direct acylation of monoglycerides. The other pathway proceeds from the acylation of α-glycerophosphate through l-α-phosphatidic acids and d-α,β-diglycerides. Ethanol is also esterified by homogenates of lactating mammary gland.

Published
1964
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4. The uptake of doubly labeled chylomicrons by guinea pig mammary gland and liver

Author

O.W. McBride and Edward D. Korn

Subjects
Biochemistry, QD415-436
Abstract

The uptake of cholesterol-H3–palmitate-C14-chylomicrons by mammary tissue and liver has been examined. The cholesterol and glyceride components of chylomicrons were taken up at the same rate by both liver and mammary tissue, as demonstrated by the unchanged ratio of C14/H3 in the tissue lipids compared to the chylomicrons. However, following injection of glycerol-C14–palmitate-H3-chylomicrons, the H3/C14 ratio of the lipids of mammary tissue was much greater than the H3/C14 ratios of the injected chylomicrons, of the serum lipids, or of the liver lipids, indicating that appreciable hydrolysis of chylomicron glycerides occurred during their uptake by mammary glands. This is consistent with the hypothesis that lipoprotein lipase is involved in the uptake of chylomicron glyceride by mammary gland.

Published
1964
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5. The lipoprotein lipase of mammary gland and the correlation of its activity to lactation

Author

O.W. McBride and Edward D. Korn

Subjects
Biochemistry, QD415-436
Abstract

The concentration of lipoprotein lipase of guinea pig mammary gland increases markedly just prior to parturition, reaching a maximal level within 2 hr post-partum. This level is maintained until the cessation of suckling, when the enzyme becomes undetectable within 18 hr. Most of the lipoprotein lipase of the mammary gland would appear to be accounted for by that in the retained milk.

Published
1963
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6. Localization of the MAGE1 gene encoding a human melanoma antigen to chromosome Xq28

Author

S. Rosenberg, R. Zakut, H. Yi, Mary G. Wang, and O.W. McBride

Subjects
X Chromosome, Chromosome Mapping, CHO Cells, In situ hybridization, Hybrid Cells, Biology, Molecular biology, Neoplasm Proteins, Xq28, Blotting, Southern, Antigen, Gene mapping, Antigens, Neoplasm, Cricetinae, Complementary DNA, Genetics, Cosmid, Animals, Humans, Cytotoxic T cell, Melanoma, Melanoma-Specific Antigens, Molecular Biology, Genetics (clinical), X chromosome
Abstract

MAGE1 encodes a tumor specific antigen MZ2-E that elicited a cytotoxic T lymphocytic response (CTL) in the patient from whom it was derived. In this study, cDNA and genomic probes have been used to localize this gene by Southern analysis of a human-rodent somatic cell hybrid panel. The probes detect a small multigene family, and both MAGEl and several other members of this family are located on the long arm of the human X chromosome. A cosmid with a 12-kb insert including the entire MAGEl gene was biotinylated and used to further localize the gene to Xq28 by in situ hybridization of metaphase spreads. The function of this antigen in normal cells and tumor cells currently remains unclear.

Published
1994
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7. Localization of two genes encoding plasma membrane Ca2+ ATPases isoforms 2 (ATP2B2) and 3 (ATP2B3) to human chromosomes 3p26→p25 and Xq28, respectively

Author

Mary G. Wang, Emanuel E. Strehler, Ernesto Carafoli, H. Hilfiker, H. Yi, and O.W. McBride

Subjects
Gene isoform, ATPase, Biology, Molecular biology, Cell biology, Gene mapping, ATP2B2, Genetic linkage, Gene expression, Genetics, biology.protein, Molecular Biology, Gene, Genetics (clinical), X chromosome
Abstract

The plasma membrane Ca2+ ATPases (PMCA) represent a highly conserved, widely dispersed, multigene family in eukaryotes consisting of at least four functional genes. The genes for PMCA isoforms 1 and 4 (ATP2B1 and ATP2B4) have been previously localized to human chromosomes 12q21→ q23 and 1q25→q32, respectively. Based upon results of fluorescence in situ hybridization (FISH), analysis of somatic cell hybrids, and genetic linkage analyses, we now report localization of ATP2B3 (PMCA isoform 3) to human chromosome Xq28, and confirm the recent localization of ATP2B2 (PMCA isoform 2) to chromosome 3p26→p25. In contrast to ATP2B1 and ATP2B4, recent studies have suggested tissue specific regulation of expression of both ATP2B2 and ATP2B3 particularly in the nervous system. The genes for several neurological and neuromuscular diseases have been assigned to the distal portion of Xq, and ATP2B3 is a candidate gene for these diseases.

Published
1994
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8. Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19

Author

O.W. McBride, Allen E. Bale, Dolph L. Hatfield, H. Harley, Thomas B. Shows, Anna L. Mitchell, Y.-S. Fan, Y. Fukushima, Byeong Jae Lee, and S.A. Rundle

Subjects
Male, Genetic Linkage, In situ hybridization, Biology, chemistry.chemical_compound, Gene mapping, Chromosome 19, Genetics, Humans, Lymphocytes, Molecular Biology, Gene, Genetics (clinical), Selenocysteine, Chromosome Mapping, Chromosome, DNA, RNA, Transfer, Amino Acid-Specific, Molecular biology, Chromosome Banding, chemistry, Genetic marker, Transfer RNA, Female, Lod Score, Chromosomes, Human, Pair 19
Abstract

The human selenocysteine tRNA gene (TRSP) has been localized on chromosome 19q13.2→q13.3 by in situ hybridization and ordered with respect to other genes and anonymous DNA markers in this region by linkage analysis in the forty CEPH pedigrees. These loci span only 10 cM in males and about 30 cM in females. The order of the loci is cen ... D19S7-D19S9-D19S47-CYP2A-CYP2F1-APOC2-(TRSP, CKM). CYP2B flanks the CYP2A and CYP2F1 loci, but it cannot be determined whether it is proximal or distal to the other two cytochrome P450 loci with respect to the centromere.

Published
1992
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9. Human interleukin 2 receptor beta-chain gene: chromosomal localization and identification of 5' regulatory sequences

Author

M.G. Wang, Warren J. Leonard, O.W. McBride, James R. Gnarra, Hiroki Otani, and Michael Sharon

Subjects
Macromolecular Substances, Chromosomes, Human, Pair 22, Molecular Sequence Data, Restriction Mapping, EcoRI, Locus (genetics), Regulatory Sequences, Nucleic Acid, Humans, Promoter Regions, Genetic, Interleukin 12 receptor, beta 1 subunit, Gene, Gene Library, Interleukin-2 Receptor beta Subunit, Regulation of gene expression, Genomic Library, Multidisciplinary, Base Sequence, biology, Chromosome Mapping, Receptors, Interleukin-2, Exons, Molecular biology, Chromosome Banding, Blotting, Southern, Genes, Regulatory sequence, Karyotyping, biology.protein, Oligonucleotide Probes, Alpha chain, Research Article
Abstract

Interleukin 2 (IL-2) binds to and stimulates activated T cells through high-affinity IL-2 receptors (IL-2Rs). Such receptors represent a complex consisting of at least two proteins, the 55-kDa IL-2R alpha chain and the 70-kDa IL-2R beta chain. The low-affinity, IL-2R alpha chain cannot by itself transduce a mitogenic signal, whereas IL-2 stimulates resting lymphocytes through the intermediate-affinity, IL-2R beta receptor. We report here identification of the genomic locus for IL-2R beta. The exons are contained on four EcoRI fragments of 1.1, 9.2, 7.2, and 13.7 kilobases. The 1.1-kilobase EcoRI fragment lies at the 5'-most end of the genomic locus and contains promoter sequences. The promoter contains no TATA box-like elements but does contain the d(GT)n class of middle repetitive elements, which may play an interesting regulatory role. The IL-2R beta gene is localized to chromosome 22q11.2-q12, a region that is the locus for several lymphoid neoplasias.

Published
1990
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10. Mapping of the gene for DNA polymerase β to mouse Chromosome 8

Author

C. A. Kozak, O.W. McBride, and S. H. Wilson

Subjects
DNA polymerase, DNA polymerase beta, Hybrid Cells, Mice, chemistry.chemical_compound, Nucleic acid thermodynamics, Gene mapping, Cricetinae, Genetics, Animals, Molecular Biology, Genetics (clinical), Polymerase, Southern blot, biology, Chromosome Mapping, Nucleic Acid Hybridization, Chromosome, DNA Polymerase I, Molecular biology, Blotting, Southern, chemistry, biology.protein, DNA polymerase I, DNA Probes, Polymorphism, Restriction Fragment Length
Abstract

We conducted Southern blot analysis of DNAs from mouse × hamster somatic cell hybrids and progeny of an interspecies backcross to localize the mouse gene for DNA polymerase β (Polb) to the centromeric end of Chromosome 8 These results provide additional support for the regional localization of polymerase β. on the short arm of human chromosome 8 or the veryproximal end of the long arm.

Published
1990
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11. Assignment of the human cyclin D3 gene (CCND3) to chromosome 6p→q13

Author

Henry M. Kronenberg, O.W. McBride, Toru Motokura, H.F. Yi, and Andrew Arnold

Subjects
biology, Cyclin D, Chromosome, Hybrid Cells, Molecular biology, Cyclin Gene, Blotting, Southern, Cyclin D1, Gene mapping, Cyclins, Multigene Family, Proto-Oncogenes, Genetics, Cancer research, biology.protein, Humans, Chromosomes, Human, Pair 6, Cloning, Molecular, Cyclin D3, Molecular Biology, Gene, Genetics (clinical), Cyclin A2, Gene Library
Abstract

The PRAD1/cyclin D1 gene (CCND1), a member of the D-type cyclin gene family, has been implicated as a protooncogene in parathyroid, lymphoid, and mammary tumors. We cloned and mapped another member of this family, the human cyclin D3 gene (CCND3), to chromosome 6p→q13 using human × rodent hybrids. This assignment raises the hypothesis that cyclin D3 may be involved in the pathogenesis of human neoplasms with abnormalities of chromosome 6.

Published
1992
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12. Cloning and chromosome mapping of human retinoid X receptor ?: selective amino acid sequence conservation of a nuclear hormone receptor in mammals

Author

K. Ozato, K. Fleischhauer, Soo Young Yang, J.P. DiSanto, and O.W. McBride

Subjects
Receptors, Retinoic Acid, Molecular Sequence Data, Receptors, Cell Surface, Hybrid Cells, Biology, Retinoid X receptor, Mice, Cricetinae, Sequence Homology, Nucleic Acid, Complementary DNA, Genetics, Animals, Humans, Amino Acid Sequence, Cloning, Molecular, Peptide sequence, Conserved Sequence, Genetics (clinical), Southern blot, Mammals, Base Sequence, Sequence Homology, Amino Acid, cDNA library, MHC Class I Gene, Nucleic acid sequence, Chromosome Mapping, Nuclear Proteins, Sequence Analysis, DNA, Blotting, Northern, Molecular biology, Retinoid X Receptors, Chromosomes, Human, Pair 6, Retinoid X receptor beta, DNA Probes, Sequence Alignment, Transcription Factors
Abstract

The murine retinoid X receptor beta (mRXR beta) is a nuclear hormone receptor that activates transcription of murine major histocompatibility complex (MHC) class I genes in response to retinoic acid. In this study, the human RXR beta gene was mapped onto the short arm or centromeric region of chromosome 6 (6pter-q13), which also harbors the MHC. Chromosomal localization was performed by Southern hybridization of genomic DNA from human rodent cell hybrids with the mRXR beta gene as a probe. In addition, a full-length cDNA clone encoding a human RXR beta was isolated by nucleic acid screening of a human cDNA library with a fragment of the mRXR beta gene as a probe. Comparison of the nucleotide-coding sequences of the human and the murine RXR beta revealed a predominance of third base substitutions, resulting in selective conservation of the predicted amino acid sequence of the proteins. The overall sequence homology was 97.6% on the amino acid level as opposed to 91.6% on the nucleotide level. In Northern hybridization experiments with the human cDNA as a probe, RXR beta gene transcripts were detected in a variety of human tumor cell lines, regardless of whether these cell lines expressed MHC class I genes.

Published
1993
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13. The CEPH consortium linkage map of human chromosome 2

Author

Nigel K. Spurr, Simon Cox, Stephen P. Bryant, John Attwood, Elizabeth B. Robson, Denis C. Shields, Todd Steinbrueck, Trefor Jenkins, Jeffrey C. Murray, Kenneth K. Kidd, Marshall L. Summar, Petros Tsipouras, Andries E. Retief, Torben A. Kruse, Allen E. Bale, Gilles Vergnaud, James L. Weber, O.W. McBride, Helen Donis-Keller, and Raymond L. White

Subjects
Genetic Linkage, Chromosomes, Human, Pair 2, Genetics, Chromosome Mapping, Humans, DNA
Abstract

This paper describes the Centre d'Etude du Polymorphisme Humain (CEPH) consortium linkage map of chromosome 2. The map contains 36 loci defined by genotyping generated from the CEPH family DNAs. A total of 73 different markers were typed by 14 contributing laboratories; of these, 36 loci are ordered on the map with likelihood support of at least 1000:1. Markers are placed along the length of the chromosome but no markers were available to anchor the map at either telomere or the centromere. Multilocus linkage analysis has produced male, female, and sex-averaged maps extending for 261, 430, and 328 cM, respectively. The sex-averaged map contains five intervals greater than 15 cM and the mean genetic distance between the 36 uniquely placed loci is 9.1 cM.

Published
1992

14. Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

Author

Sherri J. Bale, Mae R. Gailani, John J. Mulvihill, Susanna Poliak, Gary L. Peck, John J. DiGiovanna, Behram Pastakia, O.W. McBride, Mark I. Greene, David J. Leffell, Ronald G. Kase, Allen E. Bale, and M. Ann Drum

Subjects
Male, Ovarian fibroma, Heterozygote, Tumor suppressor gene, Genetic Linkage, Basal Cell Nevus Syndrome, Nevoid basal-cell carcinoma syndrome, Chromosome 9, Biology, medicine.disease, General Biochemistry, Genetics and Molecular Biology, Pedigree, Loss of heterozygosity, stomatognathic diseases, Germline mutation, Mutation, medicine, Cancer research, Humans, Basal cell carcinoma, Female, Genes, Tumor Suppressor, Chromosomes, Human, Pair 9, Polymorphism, Restriction Fragment Length
Abstract

Gorlin syndrome is an autosomal dominant disorder that predisposes to basal cell carcinomas of the skin, ovarian fibromas, and medulloblastomas. Unlike other hereditary disorders associated with cancer, it features widespread developmental defects. To investigate the possibility that the syndrome is caused by mutation in a tumor suppressor gene, we searched for loss of heterozygosity in 16 sporadic basal cell carcinomas, 2 hereditary basal cell carcinomas, and 1 hereditary ovarian fibroma and performed genetic linkage studies in five Gorlin syndrome kindreds. Eleven sporadic basal cell carcinomas and all 3 hereditary tumors had allelic loss of chromosome 9q31, and all informative kindreds showed tight linkage between the Gorlin syndrome gene and a genetic marker in this region. Loss of heterozygosity at this chromosomal location, particularly in hereditary tumors, implies that the gene is homozygously inactivated and normally functions as a tumor suppressor. In contrast, hemizygous germline mutations lead to multiple congenital anomalies.

Published
1992

15. Abstracts of workshop presentations pp. 1106-1116

Author

F. Mitelman, O.W. McBride, C. Park, F.H. Ruddle, L.L. Field, S.L. Sherman, S.T. Reeders, R.C. Douté, D. Ryan, J.M. Puck, C.E. Hildebrand, W.P. Alles, K.K. Kidd, M M Le Beau, A.M. Bowcock, R.L. Miller, M.A. Spence, T.H. Roderick, R.K. Track, G.R. Sutherland, J.-L. Mandel, D.R. Cox, M. Conneally, M.L. Mador, Frank H. Ruddle, A. Bale, E. Solomon, T.G. Berent, D.P. Doolittle, G. Romeo, A.J. Pakstis, K. Kubzdela, M.E. Hawley, T.A. Donlon, P.N. Goodfellow, R.L. Nussbaum, T.B. Shows, N. Creau-Goldberg, G.A.P Bruns, J. Weissenbach, M. Farrall, R.E. Ferrell, J.A. Rogers, M.A. FergusonSmith, K.E. Davies, A. Schinzel, J.A.M. Graves, J.J. Wasmuth, M.A. Pericak-Vance, L. Giuffra, F. Ricciuti, G.L. Schiff, A.L. Hillyard, P.J. McAlpine, M.T. Davisson, C. Junien, G. Hutchings, Y. Kaneko, D.H. Ledbetter, B. Carritt, N.E. Simpson, J. Ott, P.A. Lalley, Kenneth K. Kidd, H.S. Chan, J.E. Womack, C.T. Falk, H.-H. Ropers, D.T. Bishop, S. Povey, S.L. Naylor, H. Donis-Keller, D.W. Cox, J. Schmidtke, I.W. Craig, D.F. Barker, L.C. Stranc, L.-C. Tsui, J. Frézal, J. Gelernter, K.D. Smith, D.C. Wallace, P. Pearson, K.H. Buetow, P. Cartwright, P.S. Harper, S.J. O'Brien, M. Litt, N.K. Spurr, F. Lewitter, M.L. Cavanaugh, J.C. Murray, M. Smith, B. Keats, J.-C. Kaplan, H.F. Willard, C. Boucheix, B.S. Emanuel, and J.M. Trent

Subjects
Genetics, Library science, Biology, Molecular Biology, Genetics (clinical)
Published
1989
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16. Tight Linkage between the Syndrome of Generalized Thyroid Hormone Resistance and the Human c-erbAβ Gene

Author

Robert W. Lash, Bruce D. Weintraub, O.W. McBride, Stephen J. Usala, A.E. Bale, Neil Gesundheit, C. Weinberger, and Fredric E. Wondisford

Subjects
Genetics, Receptors, Thyroid Hormone, Thyroid hormone receptor, Genetic Linkage, Drug Resistance, Locus (genetics), Syndrome, General Medicine, Biology, medicine.disease, Thyroid Diseases, Pedigree, Gene product, Thyroid hormone resistance, Endocrinology, Nuclear receptor, Proto-Oncogene Proteins, Generalized Thyroid Hormone Resistance, medicine, Humans, Triiodothyronine, Gene family, Molecular Biology, Gene, Polymorphism, Restriction Fragment Length
Abstract

Multiple cDNAs belonging to the c-erbA gene family encode proteins that bind T3 with high affinity. However, the biological functions of these multiple thyroid hormone receptors have not yet been clarified. Generalized thyroid hormone resistance (GTHR) refers to a human syndrome characterized by tissue refractoriness to the action of thyroid hormones; several studies have suggested quantitative or qualitative defects in T3 binding to nuclear receptors in certain kindreds. To investigate the biological functions of the c-erbA genes, c-erbA alpha and c-erbA beta, we tested the hypothesis that an abnormal c-erbA gene product is present in GTHR by examining these genes in members of one kindred. Restriction enzyme analysis failed to identify an abnormal pattern in affected individuals suggesting no rearrangements or large deletions. However, we demonstrated that the gene conferring the GTHR phenotype is tightly linked to the c-erbA beta locus on chromosome 3. This linkage strongly suggests that the c-erbA beta gene is important in man as a thyroid hormone receptor and identifies a putative c-erbA beta mutant phenotype with central nervous system, pituitary, liver, metabolic, and growth abnormalities.

Published
1988
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17. Abstracts of workshop presentations pp. 1023-1039

Author

L.C. Stranc, J.M. Puck, D.R. Cox, A.L. Hillyard, P.J. McAlpine, K.K. Kidd, T.B. Shows, R.E. Ferrell, Kenneth K. Kidd, S.L. Sherman, L.L. Field, B.S. Emanuel, M.L. Cavanaugh, F.H. Ruddle, J. Weissenbach, C.E. Hildebrand, A.M. Bowcock, M. Farrall, C.T. Falk, A. Bale, E. Solomon, J.A.M. Graves, N. Creau-Goldberg, G.R. Sutherland, M. Smith, D. Ryan, B. Keats, A.J. Pakstis, G. Romeo, P.N. Goodfellow, G.A.P Bruns, M.A. Spence, M.A. FergusonSmith, J. Schmidtke, F. Mitelman, J. Ott, O.W. McBride, S. Povey, D.W. Cox, S.L. Naylor, S.T. Reeders, R.L. Miller, R.C. Douté, H. Donis-Keller, K. Kubzdela, M.E. Hawley, T.A. Donlon, C. Park, N.E. Simpson, M M Le Beau, P.A. Lalley, D.F. Barker, H.-H. Ropers, M.A. Pericak-Vance, W.P. Alles, M.L. Mador, T.H. Roderick, T.G. Berent, D.C. Wallace, R.L. Nussbaum, Y. Kaneko, D.P. Doolittle, D.T. Bishop, J.-L. Mandel, J. Frézal, J. Gelernter, K.D. Smith, J.C. Murray, J.-C. Kaplan, D.H. Ledbetter, B. Carritt, K.E. Davies, A. Schinzel, P. Cartwright, S.J. O'Brien, F. Ricciuti, M. Conneally, M.T. Davisson, C. Junien, L.-C. Tsui, H.F. Willard, C. Boucheix, P.S. Harper, M. Litt, N.K. Spurr, P. Pearson, G.L. Schiff, G. Hutchings, F. Lewitter, I.W. Craig, J.E. Womack, K.H. Buetow, R.K. Track, J.J. Wasmuth, L. Giuffra, J.M. Trent, J.A. Rogers, H.S. Chan, and Frank H. Ruddle

Subjects
Genetics, Library science, Biology, Molecular Biology, Genetics (clinical)
Published
1989
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18. Abstracts of workshop presentations pp. 1075-1091

Author

J.A. Rogers, A.J. Pakstis, G.A.P Bruns, J. Weissenbach, M. Farrall, M.L. Mador, K. Kubzdela, M.E. Hawley, T.A. Donlon, A.L. Hillyard, L.C. Stranc, D.P. Doolittle, P.J. McAlpine, J.A.M. Graves, T.B. Shows, D.W. Cox, B.S. Emanuel, F.H. Ruddle, F. Mitelman, N.E. Simpson, G.L. Schiff, J.M. Puck, K.K. Kidd, D. Ryan, Frank H. Ruddle, S.L. Sherman, G. Hutchings, S. Povey, L.L. Field, J. Ott, D.R. Cox, D.H. Ledbetter, D.C. Wallace, S.L. Naylor, R.L. Miller, H.F. Willard, J.M. Trent, C.E. Hildebrand, B. Carritt, C. Boucheix, P.A. Lalley, C. Park, T.H. Roderick, R.K. Track, M. Conneally, H. Donis-Keller, P. Pearson, D.F. Barker, H.-H. Ropers, K.H. Buetow, T.G. Berent, F. Lewitter, W.P. Alles, D.T. Bishop, P.S. Harper, M. Litt, J.J. Wasmuth, N.K. Spurr, Kenneth K. Kidd, L. Giuffra, H.S. Chan, J.-L. Mandel, C.T. Falk, J.E. Womack, J. Schmidtke, J.C. Murray, J.-C. Kaplan, R.E. Ferrell, J. Frézal, J. Gelernter, K.D. Smith, M.L. Cavanaugh, M.A. Spence, I.W. Craig, M. Smith, B. Keats, F. Ricciuti, M.T. Davisson, C. Junien, L.-C. Tsui, N. Creau-Goldberg, O.W. McBride, S.T. Reeders, R.C. Douté, M M Le Beau, P. Cartwright, S.J. O'Brien, M.A. FergusonSmith, A. Bale, E. Solomon, G. Romeo, K.E. Davies, A. Schinzel, P.N. Goodfellow, R.L. Nussbaum, A.M. Bowcock, G.R. Sutherland, M.A. Pericak-Vance, and Y. Kaneko

Subjects
Genetics, Library science, Biology, Molecular Biology, Genetics (clinical)
Published
1989
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19. Contents Vol. 51, 1989

Author

A. Bale, E. Solomon, M.A. Pericak-Vance, M. Conneally, G. Romeo, D.H. Ledbetter, B. Carritt, Y. Kaneko, P.N. Goodfellow, J.E. Womack, T.G. Berent, P.S. Harper, W.P. Alles, J. Frézal, M. Litt, N.K. Spurr, M.L. Mador, J.J. Wasmuth, J.-L. Mandel, J. Gelernter, L. Giuffra, A.J. Pakstis, F. Ricciuti, K.D. Smith, A.M. Bowcock, O.W. McBride, J. Ott, R.L. Nussbaum, S.T. Reeders, T.H. Roderick, R.C. Douté, N. Creau-Goldberg, L.L. Field, R.K. Track, M M Le Beau, G.A.P Bruns, D.P. Doolittle, G.R. Sutherland, R.E. Ferrell, F. Mitelman, C.E. Hildebrand, C.T. Falk, J.M. Trent, F.H. Ruddle, B.S. Emanuel, M.T. Davisson, N.E. Simpson, P. Pearson, M. Smith, D. Ryan, P.A. Lalley, M.A. FergusonSmith, G.L. Schiff, F. Lewitter, Frank H. Ruddle, B. Keats, A.L. Hillyard, C. Junien, G. Hutchings, I.W. Craig, P.J. McAlpine, R.L. Miller, M.A. Spence, J. Schmidtke, L.-C. Tsui, K.H. Buetow, H.S. Chan, T.B. Shows, K.E. Davies, A. Schinzel, H.-H. Ropers, D.W. Cox, P. Cartwright, S.J. O'Brien, C. Park, D.F. Barker, H.F. Willard, C. Boucheix, M.L. Cavanaugh, J. Weissenbach, M. Farrall, J.A.M. Graves, S.L. Sherman, D.R. Cox, L.C. Stranc, J.M. Puck, K.K. Kidd, K. Kubzdela, M.E. Hawley, T.A. Donlon, D.C. Wallace, H. Donis-Keller, D.T. Bishop, Kenneth K. Kidd, J.A. Rogers, S. Povey, S.L. Naylor, J.C. Murray, and J.-C. Kaplan

Subjects
Botany, Genetics, Zoology, Biology, Molecular Biology, Genetics (clinical)
Published
1989
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20. Localization of a unique DNA sequence to band p16 of human chromosome 4

Author

M.F. Singer, J. Sawyer, O.W. McBride, R.E. Thayer, and M.E. Harper

Subjects
Genetic Markers, Satellite DNA, DNA, Satellite, Hybrid Cells, Biology, DNA sequencing, chemistry.chemical_compound, Cricetulus, Cricetinae, Genetics, Animals, Humans, Genomic library, Molecular Biology, Genetics (clinical), Southern blot, Base Sequence, Nucleic acid sequence, Chromosome Mapping, Molecular biology, Chromosome Banding, Chromosome 4, chemistry, Karyotyping, Chromosomes, Human, Pair 4, Chromosome 22, DNA
Abstract

Southern blot analysis of DNA from human-rodent cell hybrids and in situ hybridization to metaphase chromosomes allowed the assignment of a unique human DNA sequence associated with satellite DNA to band p16 of human chromosome 4.

Published
1987
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21. Abstracts of workshop presentations pp. 948-967

Author

F.H. Ruddle, B.S. Emanuel, S. Povey, M.A. Pericak-Vance, D. Ryan, S.L. Naylor, K. Kubzdela, M.E. Hawley, T.A. Donlon, D.W. Cox, C. Park, D.F. Barker, Y. Kaneko, R.L. Miller, M.L. Cavanaugh, M. Smith, B. Keats, D.C. Wallace, Kenneth K. Kidd, A. Bale, N. Creau-Goldberg, M.L. Mador, A.M. Bowcock, W.P. Alles, G.R. Sutherland, J.-L. Mandel, J. Ott, E. Solomon, A.L. Hillyard, T.B. Shows, M. Conneally, T.G. Berent, J.C. Murray, J.-C. Kaplan, G. Romeo, M.A. FergusonSmith, P. Cartwright, P.J. McAlpine, D.P. Doolittle, J.M. Trent, F. Mitelman, P.N. Goodfellow, S.J. O'Brien, J.A. Rogers, H.-H. Ropers, M.A. Spence, P.A. Lalley, D.T. Bishop, N.E. Simpson, J. Frézal, T.H. Roderick, J.M. Puck, J. Gelernter, K.D. Smith, K.K. Kidd, P. Pearson, R.L. Nussbaum, O.W. McBride, S.T. Reeders, H. Donis-Keller, D.H. Ledbetter, B. Carritt, R.C. Douté, K.E. Davies, A. Schinzel, M M Le Beau, L.L. Field, F. Lewitter, C.E. Hildebrand, F. Ricciuti, M.T. Davisson, L.C. Stranc, R.E. Ferrell, C. Junien, L.-C. Tsui, I.W. Craig, J.E. Womack, K.H. Buetow, G.L. Schiff, G. Hutchings, C.T. Falk, H.F. Willard, C. Boucheix, J. Schmidtke, R.K. Track, P.S. Harper, M. Litt, H.S. Chan, N.K. Spurr, Frank H. Ruddle, J. Weissenbach, M. Farrall, J.A.M. Graves, J.J. Wasmuth, L. Giuffra, S.L. Sherman, D.R. Cox, A.J. Pakstis, and G.A.P Bruns

Subjects
Genetics, Library science, Computational biology, Biology, Molecular Biology, Genetics (clinical)
Published
1989
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22. Index by Keyword

Author

A.L. Hillyard, P.J. McAlpine, D.W. Cox, S. Povey, R.L. Nussbaum, S.L. Naylor, A. Bale, E. Solomon, G. Romeo, F. Ricciuti, D.F. Barker, P.N. Goodfellow, J.A. Rogers, L.L. Field, M.A. Spence, Frank H. Ruddle, H. Donis-Keller, C.E. Hildebrand, K. Kubzdela, M.E. Hawley, T.A. Donlon, T.G. Berent, B.S. Emanuel, M.T. Davisson, O.W. McBride, Kenneth K. Kidd, A.J. Pakstis, S.T. Reeders, R.C. Douté, M M Le Beau, C. Junien, M. Conneally, C. Park, M.A. Pericak-Vance, G.A.P Bruns, L.-C. Tsui, J.J. Wasmuth, N. Creau-Goldberg, M.L. Cavanaugh, L. Giuffra, F. Mitelman, D.C. Wallace, M. Smith, B. Keats, J. Frézal, J. Gelernter, P. Cartwright, R.E. Ferrell, M.A. FergusonSmith, K.D. Smith, S.J. O'Brien, G.L. Schiff, M.L. Mador, N.E. Simpson, Y. Kaneko, G. Hutchings, D.H. Ledbetter, T.H. Roderick, D.T. Bishop, J.M. Trent, B. Carritt, L.C. Stranc, D.P. Doolittle, J.M. Puck, K.K. Kidd, F.H. Ruddle, H.F. Willard, J.E. Womack, J.-L. Mandel, K.E. Davies, A. Schinzel, R.K. Track, S.L. Sherman, C. Boucheix, A.M. Bowcock, D. Ryan, G.R. Sutherland, R.L. Miller, T.B. Shows, P.S. Harper, M. Litt, N.K. Spurr, D.R. Cox, H.-H. Ropers, P. Pearson, F. Lewitter, K.H. Buetow, I.W. Craig, J. Weissenbach, M. Farrall, J. Ott, J.A.M. Graves, P.A. Lalley, J.C. Murray, J.-C. Kaplan, H.S. Chan, C.T. Falk, J. Schmidtke, and W.P. Alles

Subjects
Index (economics), Statistics, Genetics, Biology, Bioinformatics, Molecular Biology, Genetics (clinical)
Published
1989
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23. Abstracts of workshop presentations pp. 1006-1022

Author

A.M. Bowcock, H. Donis-Keller, G.R. Sutherland, J. Weissenbach, P. Pearson, M. Farrall, J.J. Wasmuth, A.J. Pakstis, L. Giuffra, D.W. Cox, F. Lewitter, Frank H. Ruddle, G.A.P Bruns, S. Povey, J.A.M. Graves, S.L. Naylor, M.A. Spence, J.A. Rogers, D.F. Barker, D.C. Wallace, D.R. Cox, J.C. Murray, J.-C. Kaplan, R.K. Track, N.E. Simpson, A.L. Hillyard, C.T. Falk, K.H. Buetow, P. Cartwright, M.A. Pericak-Vance, P.J. McAlpine, Kenneth K. Kidd, M. Smith, B. Keats, S.J. O'Brien, B.S. Emanuel, J. Ott, L.L. Field, H.-H. Ropers, Y. Kaneko, N. Creau-Goldberg, A. Bale, E. Solomon, J.M. Trent, C.E. Hildebrand, F. Ricciuti, H.F. Willard, G. Romeo, M.T. Davisson, C. Boucheix, P.N. Goodfellow, C. Junien, J.E. Womack, K. Kubzdela, M.E. Hawley, T.A. Donlon, S.L. Sherman, L.-C. Tsui, J. Schmidtke, D.H. Ledbetter, P.A. Lalley, D.T. Bishop, M. Conneally, B. Carritt, M.L. Cavanaugh, O.W. McBride, S.T. Reeders, R.C. Douté, P.S. Harper, W.P. Alles, M. Litt, M.A. FergusonSmith, M M Le Beau, H.S. Chan, N.K. Spurr, K.E. Davies, A. Schinzel, G.L. Schiff, T.G. Berent, R.E. Ferrell, J. Frézal, G. Hutchings, J. Gelernter, I.W. Craig, K.D. Smith, J.M. Puck, K.K. Kidd, C. Park, R.L. Nussbaum, L.C. Stranc, T.B. Shows, T.H. Roderick, F.H. Ruddle, D. Ryan, R.L. Miller, M.L. Mador, D.P. Doolittle, F. Mitelman, and J.-L. Mandel

Subjects
Genetics, Library science, Biology, Molecular Biology, Genetics (clinical)
Published
1989
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24. The lipoprotein lipase of mammary gland and the correlation of its activity to lactation

Author

Edward D. Korn and O.W. McBride

Subjects
chemistry.chemical_classification, medicine.medical_specialty, Lipoprotein lipase, Pregnancy animal, Mammary gland, Cell Biology, QD415-436, Biology, Biochemistry, Guinea pig, chemistry.chemical_compound, Endocrinology, Enzyme, medicine.anatomical_structure, chemistry, Internal medicine, Lactation, medicine, Weaning, Lactose
Abstract

The concentration of lipoprotein lipase of guinea pig mammary gland increases markedly just prior to parturition, reaching a maximal level within 2 hr post-partum. This level is maintained until the cessation of suckling, when the enzyme becomes undetectable within 18 hr. Most of the lipoprotein lipase of the mammary gland would appear to be accounted for by that in the retained milk.

Published
1963

25. Uptake of free fatty acids and chylomicron glycerides by guinea pig mammary gland in pregnancy and lactation

Author

Edward D. Korn and O.W. McBride

Subjects
medicine.medical_specialty, Pregnancy, Fetus, Chemistry, Glyceride, Mammary gland, Cell Biology, QD415-436, medicine.disease, Biochemistry, Placental Membrane, Guinea pig, Endocrinology, medicine.anatomical_structure, Internal medicine, Lactation, medicine, lipids (amino acids, peptides, and proteins), Chylomicron
Abstract

Mammary tissue of lactating guinea pigs was shown to take up both free fatty acids and chylomicron glycerides from plasma approximately twenty times more rapidly than mammary glands from midpregnant animals. The rates of removal of both forms of lipid by lactating mammary gland are comparable with those of liver. Free fatty acids cross the placental membrane and are rapidly taken up by fetuses at midpregnancy. There is no transfer of chylomicron glyceride across the placental membrane.

Published
1964

26. Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11

Author

Thomas M Glaser, O.W. McBride, Karen Stewart, Kazushige Sakaguchi, Gerald D. Aurbach, Joseph E. Green, Laura Dachowski, Maria Luisa Brandi, Stephen J. Marx, Sherri J. Bale, John J. Mulvihill, and Allen E. Bale

Subjects
Genetic Markers, Male, endocrine system, congenital, hereditary, and neonatal diseases and abnormalities, Phosphorylases, endocrine system diseases, Basic fibroblast growth factor, Locus (genetics), Biology, chemistry.chemical_compound, Glycogen phosphorylase, Genetic linkage, Genetics, medicine, Humans, MEN1, Multiple endocrine neoplasia, Gene, Chromosomes, Human, Pair 11, Multiple Endocrine Neoplasia, medicine.disease, Pedigree, chemistry, Genetic marker, Female, Lod Score, Polymorphism, Restriction Fragment Length
Abstract

We evaluated linkage between the locus for multiple endocrine neoplasia type 1 (MEN1) and several polymorphic DNA markers on chromosome 11 in a single large pedigree. On the basis of the finding of a basic fibroblast growth factor (bFGF)-like substance circulating in plasma of MEN1 patients, we chose a bFGF-related gene known to be localized to 11q13 as one of the markers. This gene locus, INT2, was found to be closely linked to the MEN1 gene. Pairwise and multipoint analyses with INT2 confirm the recent finding by C. Larsson et al. (1988, Nature (London) 332: 85–87) of MEN1 linkage to another marker, skeletal muscle glycogen phosphorylase, at 11q13.

Published
1989
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27. A retinoic acid receptor cDNA probe (RAR2) identifies a moderately frequent RFLP on chromosome 17

Author

C. Weinberger, O.W. McBride, and A.E. Bale

Subjects
Genetics, Polymorphism, Genetic, Receptors, Retinoic Acid, Retinoic acid, Chromosome Mapping, DNA, Biology, Molecular biology, Chromosome 17 (human), chemistry.chemical_compound, Retinoic acid receptor, chemistry, Gene mapping, Complementary DNA, Humans, Restriction fragment length polymorphism, Carrier Proteins, Allele frequency, Polymorphism, Restriction Fragment Length, Chromosomes, Human, Pair 17
Published
1988

29. A cDNA probe (PheA12) from the hc-(ERBA) gene on chromosome 3 detects a high frequency RFLP

Author

A.E. Bale, S. Usala, O.W. McBride, Bruce D. Weintraub, and C. Weinberger

Subjects
Genetics, Polymorphism, Genetic, Chromosome Mapping, DNA, Biology, Molecular biology, Chromosome 3, Dna genetics, Gene mapping, Complementary DNA, Proto-Oncogene Proteins, Humans, Chromosomes, Human, Pair 3, Restriction fragment length polymorphism, Molecular probe, Gene, Allele frequency, Polymorphism, Restriction Fragment Length
Published
1988

30. Index by Abstract Number

Author

F.H. Ruddle, T.B. Shows, J.E. Womack, D. Ryan, S. Povey, S.L. Naylor, W.P. Alles, A.M. Bowcock, R.L. Miller, A. Bale, E. Solomon, G.R. Sutherland, G. Romeo, T.H. Roderick, C.T. Falk, D.R. Cox, P.N. Goodfellow, P. Cartwright, S.J. O'Brien, J.-L. Mandel, M.L. Mador, L.C. Stranc, Kenneth K. Kidd, H.-H. Ropers, J. Schmidtke, J. Ott, J.M. Trent, D.P. Doolittle, M.A. Pericak-Vance, O.W. McBride, J. Weissenbach, M. Farrall, P. Pearson, A.L. Hillyard, S.T. Reeders, R.C. Douté, P.J. McAlpine, H. Donis-Keller, B.S. Emanuel, K.E. Davies, L.L. Field, M M Le Beau, F. Lewitter, A. Schinzel, F. Ricciuti, J.M. Puck, Y. Kaneko, C.E. Hildebrand, F. Mitelman, J.A.M. Graves, A.J. Pakstis, P.S. Harper, M. Litt, N.K. Spurr, M.T. Davisson, C. Junien, K.K. Kidd, L.-C. Tsui, T.G. Berent, H.S. Chan, J.J. Wasmuth, G.L. Schiff, G.A.P Bruns, P.A. Lalley, L. Giuffra, N. Creau-Goldberg, G. Hutchings, I.W. Craig, S.L. Sherman, M. Conneally, J.C. Murray, J. Frézal, J.-C. Kaplan, D.T. Bishop, K. Kubzdela, M.E. Hawley, T.A. Donlon, D.H. Ledbetter, D.C. Wallace, R.E. Ferrell, B. Carritt, J. Gelernter, M.A. FergusonSmith, K.D. Smith, M.L. Cavanaugh, D.W. Cox, H.F. Willard, M.A. Spence, C. Boucheix, R.K. Track, R.L. Nussbaum, D.F. Barker, Frank H. Ruddle, N.E. Simpson, M. Smith, B. Keats, K.H. Buetow, C. Park, and J.A. Rogers

Subjects
Index (economics), business.industry, Statistics, Genetics, Biology, business, Molecular Biology, Genetics (clinical), Biotechnology
Published
1989
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31. A new polymorphic probe on chromosome 3p: λLIB34-60 [D3S154]

Author

O.W. McBride, Gladys Glenn, Hiltrud Brauch, Farida Latif, K. Hampsch, J. Delisio, Berton Zbar, L.N. Daniel, and Michael I. Lerman

Subjects
Genetic Markers, Genetics, Hybridization probe, Chromosome, Biology, Gene mapping, Genetic marker, Humans, Chromosomes, Human, Pair 3, DNA Probes, Deoxyribonucleases, Type II Site-Specific, Molecular probe, Polymorphism, Restriction Fragment Length
Published
1989
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32. A note on the use of HGML LIT literature file numbers

Author

J.M. Trent, A. Bale, E. Solomon, F.H. Ruddle, G. Romeo, L.L. Field, P. Pearson, J.E. Womack, F. Lewitter, D. Ryan, I.W. Craig, T.B. Shows, G.L. Schiff, C.E. Hildebrand, P.N. Goodfellow, P. Cartwright, M.A. Spence, W.P. Alles, S.J. O'Brien, H.F. Willard, G. Hutchings, C. Boucheix, R.L. Miller, D.W. Cox, Frank H. Ruddle, A.M. Bowcock, H.-H. Ropers, F. Ricciuti, O.W. McBride, G.R. Sutherland, S.T. Reeders, D.F. Barker, M.L. Mador, M. Smith, M.T. Davisson, C. Junien, L.-C. Tsui, K.H. Buetow, R.E. Ferrell, R.C. Douté, M M Le Beau, M. Conneally, B. Keats, J.J. Wasmuth, L. Giuffra, D.P. Doolittle, T.H. Roderick, P.S. Harper, M.A. Pericak-Vance, B.S. Emanuel, M. Litt, N.K. Spurr, N.E. Simpson, H.S. Chan, A.J. Pakstis, M.L. Cavanaugh, C. Park, R.K. Track, J. Ott, Y. Kaneko, C.T. Falk, G.A.P Bruns, J. Frézal, J. Gelernter, K.D. Smith, J.-L. Mandel, P.A. Lalley, J. Schmidtke, K.E. Davies, A. Schinzel, A.L. Hillyard, N. Creau-Goldberg, P.J. McAlpine, S.L. Sherman, D.H. Ledbetter, F. Mitelman, M.A. FergusonSmith, B. Carritt, J. Weissenbach, M. Farrall, J.A.M. Graves, T.G. Berent, D.R. Cox, R.L. Nussbaum, L.C. Stranc, D.C. Wallace, H. Donis-Keller, Kenneth K. Kidd, J.A. Rogers, D.T. Bishop, S. Povey, S.L. Naylor, J.M. Puck, K.K. Kidd, K. Kubzdela, M.E. Hawley, T.A. Donlon, J.C. Murray, and J.-C. Kaplan

Subjects
Information retrieval, Genetics, Biology, Bioinformatics, Molecular Biology, Genetics (clinical)
Published
1989
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33. Summary of Human Gene Map, New Haven, HGM – 1, 1973, ‘Data 1'

Author

J.C. Murray, J.-C. Kaplan, K. Kubzdela, M.E. Hawley, T.A. Donlon, J. Weissenbach, M. Farrall, F. Ricciuti, M.T. Davisson, T.G. Berent, M.A. Spence, C. Junien, L.-C. Tsui, J.A.M. Graves, A.L. Hillyard, P.J. McAlpine, Frank H. Ruddle, P. Pearson, S. Povey, D.R. Cox, J.A. Rogers, F. Lewitter, W.P. Alles, D.W. Cox, P. Cartwright, S.J. O'Brien, S.L. Naylor, K.E. Davies, A. Schinzel, L.L. Field, F.H. Ruddle, A.M. Bowcock, C.E. Hildebrand, G.L. Schiff, G.R. Sutherland, D.C. Wallace, D. Ryan, R.E. Ferrell, J.J. Wasmuth, L. Giuffra, G. Hutchings, D.F. Barker, C. Park, J.M. Trent, H.-H. Ropers, H. Donis-Keller, D.T. Bishop, H.S. Chan, S.L. Sherman, M. Conneally, J.E. Womack, N.E. Simpson, J. Frézal, Kenneth K. Kidd, R.L. Miller, B.S. Emanuel, J.M. Puck, L.C. Stranc, K.K. Kidd, J. Gelernter, K.D. Smith, M.L. Cavanaugh, A.J. Pakstis, M.A. Pericak-Vance, M.L. Mador, R.K. Track, D.H. Ledbetter, B. Carritt, G.A.P Bruns, M. Smith, B. Keats, D.P. Doolittle, Y. Kaneko, C.T. Falk, J. Schmidtke, K.H. Buetow, O.W. McBride, P.S. Harper, S.T. Reeders, M. Litt, N.K. Spurr, R.C. Douté, M M Le Beau, H.F. Willard, C. Boucheix, A. Bale, E. Solomon, I.W. Craig, G. Romeo, P.N. Goodfellow, J. Ott, P.A. Lalley, N. Creau-Goldberg, M.A. FergusonSmith, R.L. Nussbaum, F. Mitelman, J.-L. Mandel, T.B. Shows, and T.H. Roderick

Subjects
Genetics, Gene map, Computational biology, Biology, Molecular Biology, Genetics (clinical), Haven
Published
1989
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34. Guidelines for interpreting abbreviations and specialized phrases in committee text and tables

Author

K. Kubzdela, M.E. Hawley, T.A. Donlon, I.W. Craig, B.S. Emanuel, N.E. Simpson, A.M. Bowcock, G.R. Sutherland, J.M. Puck, J.E. Womack, C. Park, K.K. Kidd, J.A. Rogers, W.P. Alles, H.S. Chan, J.J. Wasmuth, J. Frézal, J. Weissenbach, M.A. Pericak-Vance, P.S. Harper, L. Giuffra, M. Farrall, M.L. Mador, A.J. Pakstis, J. Gelernter, K.D. Smith, H. Donis-Keller, J. Ott, L.L. Field, R.K. Track, D.P. Doolittle, G.A.P Bruns, C.E. Hildebrand, Y. Kaneko, M. Litt, N.K. Spurr, O.W. McBride, T.H. Roderick, T.B. Shows, R.E. Ferrell, J.M. Trent, D.H. Ledbetter, F.H. Ruddle, B. Carritt, S.T. Reeders, R.C. Douté, P.A. Lalley, M M Le Beau, D. Ryan, C.T. Falk, J.A.M. Graves, M. Conneally, K.E. Davies, A. Schinzel, D.R. Cox, P. Pearson, Frank H. Ruddle, R.L. Miller, G.L. Schiff, F. Lewitter, F. Ricciuti, J. Schmidtke, T.G. Berent, H.F. Willard, J.C. Murray, J.-C. Kaplan, C. Boucheix, A. Bale, E. Solomon, M.T. Davisson, G. Hutchings, G. Romeo, C. Junien, P.N. Goodfellow, L.-C. Tsui, A.L. Hillyard, P.J. McAlpine, P. Cartwright, S.J. O'Brien, M.A. Spence, M.L. Cavanaugh, S.L. Sherman, D.W. Cox, D.C. Wallace, L.C. Stranc, K.H. Buetow, D.F. Barker, D.T. Bishop, H.-H. Ropers, M. Smith, B. Keats, S. Povey, S.L. Naylor, Kenneth K. Kidd, R.L. Nussbaum, N. Creau-Goldberg, M.A. FergusonSmith, J.-L. Mandel, and F. Mitelman

Subjects
Genetics, Biology, Molecular Biology, Genetics (clinical), Linguistics
Published
1989
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