Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 11
... interest in such problems . These two examples of nosological growth are typical of nearly all forms of hereditary disease which now occupy our interest . The result is that Dr. McKusick's ( 1968 ) catalogue of genetic disease has grown ...
... interest in such problems . These two examples of nosological growth are typical of nearly all forms of hereditary disease which now occupy our interest . The result is that Dr. McKusick's ( 1968 ) catalogue of genetic disease has grown ...
Seite 216
... interest ' ( Lillie , 1916 ) , eludes us with respect to its precise pathogenesis . Several other aspects of blood chimerism have been of recent interest . Thus , it has been observed that the admixture ratio in the chimeric twins ...
... interest ' ( Lillie , 1916 ) , eludes us with respect to its precise pathogenesis . Several other aspects of blood chimerism have been of recent interest . Thus , it has been observed that the admixture ratio in the chimeric twins ...
Seite 223
... interest is the mechanics of how chimeric individuals come about . Most papers and reviews dealing with this subject have enumerated the possibilities at length and it may thus be forgiven if I do not review polyandry , polygyny , etc ...
... interest is the mechanics of how chimeric individuals come about . Most papers and reviews dealing with this subject have enumerated the possibilities at length and it may thus be forgiven if I do not review polyandry , polygyny , etc ...
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