Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 155
... selection and mutation * I should like to discuss three aspects of human population genetics . The first of these is the demographic framework , the pattern of birth and death rates , within which natural selection operates . Secondly ...
... selection and mutation * I should like to discuss three aspects of human population genetics . The first of these is the demographic framework , the pattern of birth and death rates , within which natural selection operates . Secondly ...
Seite 159
... selection . Postnatal , prereproductive death rates are now very low in many countries . The opportu- nity for selection through this mechanism is far less than in the past and there is every reason to think that this represents a real ...
... selection . Postnatal , prereproductive death rates are now very low in many countries . The opportu- nity for selection through this mechanism is far less than in the past and there is every reason to think that this represents a real ...
Seite 161
... selection within families , which is what would occur with perfect reproductive compensation , should change the phenotypic average just as fast as if there were zero compensation . The effect of relaxed selection for more complexly ...
... selection within families , which is what would occur with perfect reproductive compensation , should change the phenotypic average just as fast as if there were zero compensation . The effect of relaxed selection for more complexly ...
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