Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 356
... inheritance would be exclud- ed if the first interpretation were correct must therefore be examined . I believe that ... inheritance . The following are some well documented examples : 1. Human serum proteins : People with inherited ...
... inheritance would be exclud- ed if the first interpretation were correct must therefore be examined . I believe that ... inheritance . The following are some well documented examples : 1. Human serum proteins : People with inherited ...
Seite 357
... inheritance ( Schultz , 1970 ) . However , the result of a preliminary analysis ( Edwards , 1960 ) seems to suggest that her family data may not fit polygenic inheritance any better than they do simple inheritance . Polygenic inheritance ...
... inheritance ( Schultz , 1970 ) . However , the result of a preliminary analysis ( Edwards , 1960 ) seems to suggest that her family data may not fit polygenic inheritance any better than they do simple inheritance . Polygenic inheritance ...
Seite 384
... INHERITANCE An interesting development in pharmacogenetics has been the use of twin studies in at- tempting to define genetic factors in drug metabolism . It is somewhat paradoxical that , as twin studies have somewhat gone out of ...
... INHERITANCE An interesting development in pharmacogenetics has been the use of twin studies in at- tempting to define genetic factors in drug metabolism . It is somewhat paradoxical that , as twin studies have somewhat gone out of ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
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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