Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 136
... correlation coefficients , for likeness between relatives for additive characters , are reduced according to the magnitude of the selection coefficient . For example , for perfectly additive gene effects ( Penrose , 1964 ) , ( parent ...
... correlation coefficients , for likeness between relatives for additive characters , are reduced according to the magnitude of the selection coefficient . For example , for perfectly additive gene effects ( Penrose , 1964 ) , ( parent ...
Seite 268
... correlation , often quite substantial , between Levels I and II . But correlation does not necessarily imply functional dependence of one set of pro- cesses upon another , in this case Level II upon Level 1. This question has puzzled us ...
... correlation , often quite substantial , between Levels I and II . But correlation does not necessarily imply functional dependence of one set of pro- cesses upon another , in this case Level II upon Level 1. This question has puzzled us ...
Seite 405
... correlate rates of metabolism of phenylbutazone , antipyrine , bishydroxycoumarin and ethanol . The only correlation between the plasma half - lives of these drugs after a single oral dose of each was between rates of metabolism of ...
... correlate rates of metabolism of phenylbutazone , antipyrine , bishydroxycoumarin and ethanol . The only correlation between the plasma half - lives of these drugs after a single oral dose of each was between rates of metabolism of ...
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