Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 28
... similar in all the cultures , although other experiments showed that the growth of the cells from the patients with citrullinemia and argininosuccinic aciduria subsequently slowed in arginine - deficient medium . C14 - citrulline ...
... similar in all the cultures , although other experiments showed that the growth of the cells from the patients with citrullinemia and argininosuccinic aciduria subsequently slowed in arginine - deficient medium . C14 - citrulline ...
Seite 217
... similar unusual placenta without , however , demonstrating chimerism in the twins . A more detailed study of fraternal twins is thus warranted in the future . Clearly , isosexual chimeras must exist as frequently but only one such ...
... similar unusual placenta without , however , demonstrating chimerism in the twins . A more detailed study of fraternal twins is thus warranted in the future . Clearly , isosexual chimeras must exist as frequently but only one such ...
Seite 407
... similar bishydroxycoumarin half - lives , one indi- vidual did not smoke , whereas the other consumed two packs a day . Additional discordant ex- amples occurred for both smoking and coffee consumption . To determine whether a relation ...
... similar bishydroxycoumarin half - lives , one indi- vidual did not smoke , whereas the other consumed two packs a day . Additional discordant ex- amples occurred for both smoking and coffee consumption . To determine whether a relation ...
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