Author: "ten Kate LP" / Publication Year Range: More than 50 years ago - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"ten Kate LP"' showing total 7 results

Start Over Author "ten Kate LP" Publication Year Range More than 50 years ago

7 results on '"ten Kate LP"'

1. Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.

Author: Gouw WL, Anders GJ, ten Kate LP, and de Groot CJ
Subjects: Abnormalities, Multiple, Blood Group Antigens, Child, Preschool, Chromosome Aberrations, Chromosomes, Human, 13-15, Dermatoglyphics, Female, Humans, Infant, Infant, Newborn, Karyotyping, Male, Mitosis, Pedigree, Phenotype, Pregnancy, Chromosomes, Human, 4-5, Intellectual Disability genetics, Trisomy
Published: 1972
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2. Combined deficiency of factor V and factor VIII: report of a family and genetic analysis.

Author: Sibinga CT, Gökemeyer JD, ten Kate LP, and Bos-van Zwol F
Subjects: Adolescent, Adult, Aged, Blood Coagulation Disorders complications, Blood Coagulation Tests, Factor V Deficiency complications, Female, Genes, Recessive, Heterozygote, Homozygote, Humans, Male, Middle Aged, Pedigree, Sex Factors, Blood Coagulation Disorders genetics, Factor V Deficiency genetics, Factor VIII
Published: 1972
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3. Serum dependency of cellular phenotype in mucopolysaccharidoses: the influence of autologous serum on metachromasia.

Author: ten Kate LP, Anders GJ, and de Groot CJ
Subjects: Animals, Biopsy, Cattle, Cells, Cultured, Culture Media, Fetus, Fibroblasts, Humans, Mucopolysaccharidoses pathology, Phenotype, Plasma, Skin pathology, Carbohydrate Metabolism, Inborn Errors, Glycosaminoglycans, Intellectual Disability, Mucopolysaccharidoses genetics
Published: 1973
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4. Neurofibromatosis with mandibular deformities.

Author: Rittersma J, ten Kate LP, and Westerink P
Subjects: Adolescent, Female, Humans, Jaw Abnormalities diagnostic imaging, Jaw Abnormalities genetics, Maxilla abnormalities, Maxillofacial Development, Middle Aged, Neurofibromatosis 1 genetics, Pedigree, Radiography, Zygoma abnormalities, Jaw Abnormalities complications, Mandible abnormalities, Neurofibromatosis 1 complications
Published: 1972
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5. A case of 18q-in a family with a translocation t(6p+;18q-), identified by the Giemsa-banding technique.

Author: Gouw WL, ten Kate LP, Anders GJ, and Okken A
Subjects: Abnormalities, Multiple genetics, Chromosome Aberrations pathology, Chromosome Disorders, Cytogenetics, Dermatoglyphics, Heterozygote, Humans, Infant, Newborn, Karyotyping, Male, Pedigree, Chromosome Aberrations diagnosis, Chromosomes, Human, 16-18
Published: 1973
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6. Unilateral agenesis of the diaphragm.

Author: ten Kate LP and Anders GJ
Subjects: Female, Genes, Recessive, Humans, Male, Parity, Pregnancy, Diaphragm abnormalities
Published: 1970
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7. Fibroblast culture in Werner's syndrome.

Author: Nienhaus AJ, de Jong B, and ten Kate LP
Subjects: Arm, Autoradiography, Breast, Cells, Cultured, Female, Humans, In Vitro Techniques, Middle Aged, Skin pathology, Thymidine, Tritium, Fibroblasts, Werner Syndrome
Published: 1971
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