Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 115
... less frequent than is characteristic of present populations which on cultural and historical grounds may be assumed to be non - contracepting and free of venereal disease . For example , some 3.4 % of ever - married Hutterite women of ...
... less frequent than is characteristic of present populations which on cultural and historical grounds may be assumed to be non - contracepting and free of venereal disease . For example , some 3.4 % of ever - married Hutterite women of ...
Seite 159
... less certain . There are known genetic conditions that cause sterility or reduced fertility , but these account for only a minute fraction of the total variability in family size . Although there are undoubtedly genet- ic factors that ...
... less certain . There are known genetic conditions that cause sterility or reduced fertility , but these account for only a minute fraction of the total variability in family size . Although there are undoubtedly genet- ic factors that ...
Seite 268
... less culturally biased than the IQ tests . This culture - bias hypothesis seems untenable in view of the fact that in the range of IQ above 100 , low SES children perform relatively less well on Level I tests . Also , when we have given ...
... less culturally biased than the IQ tests . This culture - bias hypothesis seems untenable in view of the fact that in the range of IQ above 100 , low SES children perform relatively less well on Level I tests . Also , when we have given ...
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