Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 164
... produced about 5 % heterozygous depression of viability per treated chromo- some , but the frequency of lethals is ... producing loci ( Shannon et al . , 1970 ) . The region appears to have been saturated , for no new mutant that does ...
... produced about 5 % heterozygous depression of viability per treated chromo- some , but the frequency of lethals is ... producing loci ( Shannon et al . , 1970 ) . The region appears to have been saturated , for no new mutant that does ...
Seite 239
... producing aneuploid gametes , depending on the chromosomes involved , the position of the break - points and the meiotic configuration . Furthermore , the probability that any aneuploid gametes produced will give rise to a recognisable ...
... producing aneuploid gametes , depending on the chromosomes involved , the position of the break - points and the meiotic configuration . Furthermore , the probability that any aneuploid gametes produced will give rise to a recognisable ...
Seite 273
... produced in this way . Furthermore , they may be expected to differ in their properties one from another , according to the particular amino- acid which has been substituted and the particular site in the protein where the substitution ...
... produced in this way . Furthermore , they may be expected to differ in their properties one from another , according to the particular amino- acid which has been substituted and the particular site in the protein where the substitution ...
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