Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 88
... migration , which was carried out by asking birth places of the individuals sampled and of their parents . Rare long distance migrants are occasionally observed but are too few for measuring the migration between areas far apart such as ...
... migration , which was carried out by asking birth places of the individuals sampled and of their parents . Rare long distance migrants are occasionally observed but are too few for measuring the migration between areas far apart such as ...
Seite 119
... migration assumes that mutation and selection are small compared with the effects of migration . One finds , for example , assertions such as the following ( Fried- laender , 1971 ) : ' Within Bougainville , the high estimates of a and ...
... migration assumes that mutation and selection are small compared with the effects of migration . One finds , for example , assertions such as the following ( Fried- laender , 1971 ) : ' Within Bougainville , the high estimates of a and ...
Seite 132
... migration , but also to mutation and normalizing selection . Wright's concept of neighbourhood size , defined in terms of the variance of migration , does not correspond to local populations , whereas Malécot's recognition of kinship as ...
... migration , but also to mutation and normalizing selection . Wright's concept of neighbourhood size , defined in terms of the variance of migration , does not correspond to local populations , whereas Malécot's recognition of kinship as ...
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