432 results on '"Lindsten J"'
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2. A Chiasma Map of Man
3. A Mapping Function for Man
4. Evidence for a Major Locus as Well as a Multifactorial Component in the Regulation of Human Red Blood Cell Catechol-O-Methyl-Transferase Activity
5. Standard Outline for Each Nation (2.1–2.19)
6. Cytogenetic Aspects of Human Male Meiosis
7. The 11q;22q translocation: A European collaborative analysis of 43 cases
8. The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families
9. The “Cat Eye syndrome”: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter→q11) associated with a characteristic phenotype: Report of 11 patients and delineation of the clinical picture
10. Changes in the incidence of Down syndrome in Sweden during 1968–1982
11. Sex-reversed XY females with campomelic dysplasia are H-Y negative
12. Correlation between the number of sex chromosomes and the H-Y antigen titer
13. Contributors to This Volume
14. Contributors
15. Methodological Aspects on the Estimation of Genetic Effects of Environmental Agents in Man
16. THE NATURE, ORIGIN, AND GENETIC IMPLICATIONS OF STRUCTURAL ABNORMALITIES OF THE SEX CHROMOSOMES IN MAN
17. THE CHROMOSOMES OF THE ALPINE MARMOT MARMOTA MARMOTA L. (RODENTIA: SCIURIDAE)1
18. The chromosomes of the Cynomolgus macaque (Macaca fascicularis)
19. Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis
20. DNA REPLICATION PATTERNS OF CANINE CHROMOSOMES IN VIVO AND IN VITRO
21. STABILITY OF ABNORMAL KARYOTYPES IN CELL CULTURE1
22. Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblasts leukemia
23. Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal
24. Diagnostic transcervical chorionic biopsles in first trimester pregnancies
25. A linkage study of the locus for X-linked Charcot-Marie-Tooth disease
26. Elevated levels of alfa fetoprotein in maternal serum and amniotic fluid in two cases of spina bifida
27. Segregation analysis of balanced pericentric inversions in pedigree data
28. Evidence for an autosomal recessive gene regulating the persistence of the insulin response to glucose in man
29. Maternal smoking and irradiation during pregnancy as risk factors for child leukemia
30. Iron malabsorption and hypochromic anemia in a case of Turner's syndrome
31. The origin and phenotype of XO males
32. Chromosomes in leukemia.
33. A Description of Nine Systems Together with Some Recommendations.
34. Late side effects of chemotherapy in ovarian carcinoma: a cytogenetic, hematologic, and statistical study.
35. European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures.
36. Section 2: Chromosome disease.
37. A family study of genetic and environmental factors determining polymorphic hydroxylation of debrisoquin.
38. The Distribution of the Gene for the Juvenile Type of Gaucher Disease in Sweden.
39. Segregation analysis of balanced pericentric inversions in pedigree data.
40. Genetic regulation of the kinetics of glucose-induced insulin release in man Studies in families with diabetic and non-diabetic probands.
41. Genetic regulation of the red cell uroporphyrinogen-l-synthetase level in families with acute intermittent porphyria.
42. Evidence for an autosomal recessive gene regulating the persistence of the insulin response to glucose in man.
43. Alpha fetoprotein levels in maternal serum and in amniotic fluid from early normal pregnancies.
44. Elevated levels of alfa fetoprotein in maternal serum and amniotic fluid in two cases of spina bifida.
45. A linkage study of the locus for X-linked Charcot-Marie-Tooth disease.
46. DNA and chromosome alterations in lymphocytes of operating room personnel and in patients before and after inhalation anaesthesia.
47. INVOLVEMENT OF CHROMOSOMES 8, 9, 19 AND 22 IN PH1 POSITIVE AND PH1 NEGATIVE CHRONIC MYELOCYTIC LEUKEMIA IN THE CHRONIC OR BLASTIC STAGE.
48. Clinical and Cytogenetic Investigation in Children of Parents Treated with Radioiodine.
49. TRISOMY 13-15.
50. Hearing Defects in Males with Sex Chromosome Anomalies.
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