Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 55
... important elements in the genetic diseases of man to which I would like to direct attention . The questions on which there is still the greatest doubt have to do with : a . how important we think the genetic component in human disease ...
... important elements in the genetic diseases of man to which I would like to direct attention . The questions on which there is still the greatest doubt have to do with : a . how important we think the genetic component in human disease ...
Seite 92
... important to allow a regular cline of genetic differences to be observed . But it should be noted that the fact that Basques show important genetic differences from the rest of Europeans ( Mourant , 1954 ) is in agreement with the idea ...
... important to allow a regular cline of genetic differences to be observed . But it should be noted that the fact that Basques show important genetic differences from the rest of Europeans ( Mourant , 1954 ) is in agreement with the idea ...
Seite 201
... important difference that there are normally only 23 of them and also that they show relic coiling . The coiling and irregular condensation of the chromatids make karyotyping difficult . However , the more obvious chromosomes can often ...
... important difference that there are normally only 23 of them and also that they show relic coiling . The coiling and irregular condensation of the chromatids make karyotyping difficult . However , the more obvious chromosomes can often ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
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Häufige Begriffe und Wortgruppen
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