Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 156
... mean number of descendants . It is invariant with respect to the total rate of growth of the population , depending only on the relative fitnesses of the different individuals in the population . The Index of Opportunity for Selection ...
... mean number of descendants . It is invariant with respect to the total rate of growth of the population , depending only on the relative fitnesses of the different individuals in the population . The Index of Opportunity for Selection ...
Seite 250
... means of verbal , performance and full - scale 7 - year IQs of twins and singletons by race Twins Singletons Difference in means Mean SD Mean SD White Verbal scale 96.0 14.3 100.0 13.7 -4.0 Performance scale 101.5 13.4 103.8 14.4 -2.3 ...
... means of verbal , performance and full - scale 7 - year IQs of twins and singletons by race Twins Singletons Difference in means Mean SD Mean SD White Verbal scale 96.0 14.3 100.0 13.7 -4.0 Performance scale 101.5 13.4 103.8 14.4 -2.3 ...
Seite 253
... Means and standard deviations of IQs of concordant , and retarded and non - retarded among discordant twins Both twins retarded One twin retarded Mean SD Retarded twin Mean SD Non - retarded twin Mean SD Twins Monozygotic 60.0 6.9 64.5 ...
... Means and standard deviations of IQs of concordant , and retarded and non - retarded among discordant twins Both twins retarded One twin retarded Mean SD Retarded twin Mean SD Non - retarded twin Mean SD Twins Monozygotic 60.0 6.9 64.5 ...
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