Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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... phenotypes with exactly the same underlying mutation . Thus , hemoglobin C disease and sickle cell disease would be ... phenotype . To describe a patient as a case of mongolism , though widely practised , is some- what misleading . A ...
... phenotypes with exactly the same underlying mutation . Thus , hemoglobin C disease and sickle cell disease would be ... phenotype . To describe a patient as a case of mongolism , though widely practised , is some- what misleading . A ...
Seite 281
... phenotype distribution in various populations . The frequencies of several variants are so high that the Pi system fulfils the requirements of a true poly- morphism . Table 3 gives the Pi gene frequencies in the same populations . In ...
... phenotype distribution in various populations . The frequencies of several variants are so high that the Pi system fulfils the requirements of a true poly- morphism . Table 3 gives the Pi gene frequencies in the same populations . In ...
Seite 496
... phenotype frequencies , 280 , 282 phenotypes , 277-280 polymorphism , 277-285 selection , 283 sex chromosome aberration , 283 polygenic inheritance oral anticoagulants response , 428-430 pharmacogenetics , 384 , 385 polygyny South ...
... phenotype frequencies , 280 , 282 phenotypes , 277-280 polymorphism , 277-285 selection , 283 sex chromosome aberration , 283 polygenic inheritance oral anticoagulants response , 428-430 pharmacogenetics , 384 , 385 polygyny South ...
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