Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 58
... associated with exencephaly , is characteristic of certain translocations . The mean frequency of extra embryonic death associated with translocation heterozygotes has tended to be slightly over 50 % . This indicates that the 50 ...
... associated with exencephaly , is characteristic of certain translocations . The mean frequency of extra embryonic death associated with translocation heterozygotes has tended to be slightly over 50 % . This indicates that the 50 ...
Seite 236
... associated with a chromosome abnormality . When data obtained from the newborn are combined with that obtained from spontaneous abortions we can conclude that some 7 % of all recognised conceptions in man are associated with a ...
... associated with a chromosome abnormality . When data obtained from the newborn are combined with that obtained from spontaneous abortions we can conclude that some 7 % of all recognised conceptions in man are associated with a ...
Seite 241
... associated with Down's syndrome , it must mean that the risk of aneuploid offspring to the carriers of such translocations is considerably lower than that previously estimated . However , it may be that , even within each individual ...
... associated with Down's syndrome , it must mean that the risk of aneuploid offspring to the carriers of such translocations is considerably lower than that previously estimated . However , it may be that , even within each individual ...
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