Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 424
... subjects with individual differences in response , but genetic investigations have not been performed . Thus , in some subjects , the use of succinylcholine is followed by muscle pain ( Bush and Roth , 1961 ; Cooke et al . , 1963 ) ...
... subjects with individual differences in response , but genetic investigations have not been performed . Thus , in some subjects , the use of succinylcholine is followed by muscle pain ( Bush and Roth , 1961 ; Cooke et al . , 1963 ) ...
Seite 433
... subjects and the propositi of kin- dreds M and McC . The response is expressed on a linear scale as the maximum ... subjects ( Fig . 7 ) , is shown here . On the abscissa are the blood levels of warfarin at 48 hours with the 99 ...
... subjects and the propositi of kin- dreds M and McC . The response is expressed on a linear scale as the maximum ... subjects ( Fig . 7 ) , is shown here . On the abscissa are the blood levels of warfarin at 48 hours with the 99 ...
Seite 439
... SUBJECTS 1500/50 = 30 RESISTANT SUBJECT 120/80 = 11⁄2 1,000 100 VITAMIN K 750 ΙΝ με 500 250- ANTICOAGULATION V. K DEFICIENCY 75 50 25 Fig . 15. The vitamin K required to reverse hypoprothrombinemia expected by long - term therapy with ...
... SUBJECTS 1500/50 = 30 RESISTANT SUBJECT 120/80 = 11⁄2 1,000 100 VITAMIN K 750 ΙΝ με 500 250- ANTICOAGULATION V. K DEFICIENCY 75 50 25 Fig . 15. The vitamin K required to reverse hypoprothrombinemia expected by long - term therapy with ...
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