108 results on '"Lindsten J"'
Search Results
2. Contributors
3. Methodological Aspects on the Estimation of Genetic Effects of Environmental Agents in Man
4. Standard Outline for Each Nation (2.1–2.19)
5. THE NATURE, ORIGIN, AND GENETIC IMPLICATIONS OF STRUCTURAL ABNORMALITIES OF THE SEX CHROMOSOMES IN MAN
6. Cytogenetic Aspects of Human Male Meiosis
7. THE NATURE, ORIGIN, AND GENETIC IMPLICATIONS OF STRUCTURAL ABNORMALITIES OF THE SEX CHROMOSOMES IN MAN
8. THE CHROMOSOMES OF THE ALPINE MARMOT MARMOTA MARMOTA L. (RODENTIA: SCIURIDAE)1
9. The chromosomes of the Cynomolgus macaque (Macaca fascicularis)
10. Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis
11. DNA REPLICATION PATTERNS OF CANINE CHROMOSOMES IN VIVO AND IN VITRO
12. STABILITY OF ABNORMAL KARYOTYPES IN CELL CULTURE1
13. Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblasts leukemia
14. Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal
15. Diagnostic transcervical chorionic biopsles in first trimester pregnancies
16. A linkage study of the locus for X-linked Charcot-Marie-Tooth disease
17. Elevated levels of alfa fetoprotein in maternal serum and amniotic fluid in two cases of spina bifida
18. Segregation analysis of balanced pericentric inversions in pedigree data
19. Evidence for an autosomal recessive gene regulating the persistence of the insulin response to glucose in man
20. The Distribution of the Gene for the Juvenile Type of Gaucher Disease in Sweden
21. A new variant translocation (19q+, 22q−) in chronic myelocytic leukemia
22. Correlation between the number of sex chromosomes and the H-Y antigen titer
23. Chromosomes in leukemia
24. A Chiasma Map of Man
25. The 11q;22q translocation: A European collaborative analysis of 43 cases
26. First trimester biopsies of chorionic villi for prenatal diagnosis: experience of two laboratories
27. Sex-reversed XY females with campomelic dysplasia are H-Y negative
28. Genetic regulation of the kinetics of glucose‐induced insulin release in man Studies in families with diabetic and non‐diabetic probands
29. DNA and Chromosome Alterations in Lymphocytes of Operating Room Personnel and in Patients before and after Inhalation Anaesthesia
30. Prenatal Cytogenetic Diagnosis
31. Clonal Origin of the Philadelphia Chromosome From Either the Paternal or the Maternal Chromosome Number 22
32. A genetic analysis of the normal body-height growth and dental development in man
33. Methylmercury-induced chromosome damage in man
34. Trisomy 8 in Acute Myeloblastic Leukemia and Sideroachrestic Anemia
35. The ?Cat Eye syndrome?: Dicentric small marker chromosome probably derived from a No. 22 (Tetrasomy 22pter?q11) associated with a characteristic phenotype
36. Iron malabsorption and hypochromic anemia in a case of Turner's syndrome
37. Alpha fetoprotein levels in maternal serum and in amniotic fluid from early normal pregnancies
38. Evidence for a Major Locus as Well as a Multifactorial Component in the Regulation of Human Red Blood Cell Catechol-O-Methyl-Transferase Activity
39. A family study of genetic and environmental factors determining polymorphic hydroxylation of debrisoquin
40. The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families
41. A Mapping Function for Man
42. Molecular forms and activities of glycosidases in cultures of amniotic-fluid cells
43. DNA repair and frequency of X-ray and u.v.-light induced chromosome aberrations in leukocytes from patients with Down's syndrome
44. CHROMOSOME ABERRATIONS AND SISTER-CHROMATID EXCHANGE IN WORKERS IN CHEMICAL LABORATORIES AND A ROTOPRINTING FACTORY AND IN CHILDREN OF WOMEN LABORATORY WORKERS
45. Changes in the incidence of Down syndrome in Sweden during 1968?1982
46. A Description of Nine Systems Together with Some Recommendations
47. Segregation of ACP1and MNSs in families with structural rearrangements involving chromosome 2
48. Section 2: Chromosome disease
49. Surveillance of Down’s Syndrome as a Paradigm of Population Monitoring
50. European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.