Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 80
Seite 222
... et al . ( 1964 ) 4. Biggers and McFeeley ( 1966 ) 38 XX / 39 XXY 5. Malouf et al . ( 1967 ) 6. Thuline ( 1964 ) 62/209 2/13 38 XX / XY Some spermatogenesis 37/59 38 XX / XY 7. Jones ( 1969 ) 38 XX / XY / 39 XXY / 40 XXYY 8. Jones ( 1969 ) ...
... et al . ( 1964 ) 4. Biggers and McFeeley ( 1966 ) 38 XX / 39 XXY 5. Malouf et al . ( 1967 ) 6. Thuline ( 1964 ) 62/209 2/13 38 XX / XY Some spermatogenesis 37/59 38 XX / XY 7. Jones ( 1969 ) 38 XX / XY / 39 XXY / 40 XXYY 8. Jones ( 1969 ) ...
Seite 446
... et al . , 1969 ) or man - Chinese hamster ( Káo and Puck , 1970 ) does not require heterozygosity at the human loci ... et al . , 1971b Chalmers and Lawler , 1953 ; Weitkamp et al . , 1970a ; Westerveld and Meera Khan , 1971 ; Renwick ...
... et al . , 1969 ) or man - Chinese hamster ( Káo and Puck , 1970 ) does not require heterozygosity at the human loci ... et al . , 1971b Chalmers and Lawler , 1953 ; Weitkamp et al . , 1970a ; Westerveld and Meera Khan , 1971 ; Renwick ...
Seite 449
... et al . , 1969 ) , the estimates for ABO / nail - patella and ABO / AK cover the same region of the chromosome . The ... et al . , 1966 ; Renwick , 1968 4. ABO / AK 0.17 0.10 1.70 Renwick , 1968 ; Weitkamp et al . , 1971b 5. 6 - PGD / Rh ...
... et al . , 1969 ) , the estimates for ABO / nail - patella and ABO / AK cover the same region of the chromosome . The ... et al . , 1966 ; Renwick , 1968 4. ABO / AK 0.17 0.10 1.70 Renwick , 1968 ; Weitkamp et al . , 1971b 5. 6 - PGD / Rh ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
17 weitere Abschnitte werden nicht angezeigt.
Häufige Begriffe und Wortgruppen
abnormal Acad acid activity alleles analysis aneuploid anti anticoagulant anticorps antigen antipyrine autosomal biochemical bishydroxycoumarin blood cell hybrids cell lines chimerism clinical clones culture Cytogenetics deficiency dehydrogenase detected deux diagnosis dose drug metabolism effect electrophoretic enzyme assay estimate été être factors Fagerhol female fibroblasts fraction G6PD gamètes gène genetic genetic control génétique hereditary heterozygotes heterozygous hexosaminidase HL-A human chromosomes individuals inheritance isozymes karyotype Level linkage lipoprotein loci locus Lp(a Lp(a+ lymphocytes lymphoid cell male marker meiosis meiotic mental retardation mouse mutation Nature Lond Negro normal observed pairs parents patients patterns peut pharmacogenetics phenotype phenylbutazone plasma polymorphism population possible Proc produit propositus protein prothrombin Pygmies rearrangement recombination red cells sera serum sibship singletons somatic cell structure studies syndrome Table Tay-Sachs disease tests tion tissues translocations twins variants Vesell vitamin vitamin K warfarin X chromosome XX/XY