Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 274
... deficiency . What we would like to know is how many actually occur among the individual members of human populations , what is their incidence and distribution , and what are their functional effects . In fact a very large number of ...
... deficiency . What we would like to know is how many actually occur among the individual members of human populations , what is their incidence and distribution , and what are their functional effects . In fact a very large number of ...
Seite 383
... deficiency and pseudocholinesterase deficiency , these include polymorphisms in acetylation of INH and related drugs ( Evans et al . , 1960 ) , drug induced hemolytic anemia due to Hb Zurich and some other unstable hemoglobins ...
... deficiency and pseudocholinesterase deficiency , these include polymorphisms in acetylation of INH and related drugs ( Evans et al . , 1960 ) , drug induced hemolytic anemia due to Hb Zurich and some other unstable hemoglobins ...
Seite 387
... deficiency of hospital patients and various other groups exposed to antimalarial therapy would avoid some hemolytic episodes . For instance , the U.S. Army does not screen but repatriates soldiers with primaquine induced hemolysis from ...
... deficiency of hospital patients and various other groups exposed to antimalarial therapy would avoid some hemolytic episodes . For instance , the U.S. Army does not screen but repatriates soldiers with primaquine induced hemolysis from ...
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