Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 64
... estimated , then it will become possible to estimate rates of induction by using the appropriate doubling dose ( Lüning and Searle , 1971 ) . Let us now consider briefly how one would expect these or other risk estimates based on acute ...
... estimated , then it will become possible to estimate rates of induction by using the appropriate doubling dose ( Lüning and Searle , 1971 ) . Let us now consider briefly how one would expect these or other risk estimates based on acute ...
Seite 119
... estimate ) to 0.00437 ( Switzerland , Alpine area , density- adjusted estimate ) have been reported ( for a summary see Imaizumi and Morton , 1969 ) . Possibly this is to be expected given the sizes of the local populations and their ...
... estimate ) to 0.00437 ( Switzerland , Alpine area , density- adjusted estimate ) have been reported ( for a summary see Imaizumi and Morton , 1969 ) . Possibly this is to be expected given the sizes of the local populations and their ...
Seite 444
... estimating map - distances conditional on synteny . If , as in counselling , we should require an estimate of the recombination fraction or proportion , we translate back from this estimate of map - distance . The data for formal ...
... estimating map - distances conditional on synteny . If , as in counselling , we should require an estimate of the recombination fraction or proportion , we translate back from this estimate of map - distance . The data for formal ...
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