Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 85
Seite 188
... blood , both from patients with various diseases and congenital abnormalities and from nor- mal persons , provides a unique opportunity for accelerating human genetic research . In the last few years we have established over 700 human ...
... blood , both from patients with various diseases and congenital abnormalities and from nor- mal persons , provides a unique opportunity for accelerating human genetic research . In the last few years we have established over 700 human ...
Seite 396
... blood concentra- tions of drug 3 , a very broad unimodal distribution may conceal heterogeneity , which can be occasionally unmasked by application of more sophisticated assay systems . For many drugs , a direct relationship exists ...
... blood concentra- tions of drug 3 , a very broad unimodal distribution may conceal heterogeneity , which can be occasionally unmasked by application of more sophisticated assay systems . For many drugs , a direct relationship exists ...
Seite 488
... blood clotting factor XII chromosome 6 , 463 blood group stature , Pygmies , 86 Yanomama Indians , 103- 105 , 107 blood group ABO system Cis AB complex , 315-329 yaws , Pygmies , 89 blood group Duffy system chromosome 1 , 461 genetic ...
... blood clotting factor XII chromosome 6 , 463 blood group stature , Pygmies , 86 Yanomama Indians , 103- 105 , 107 blood group ABO system Cis AB complex , 315-329 yaws , Pygmies , 89 blood group Duffy system chromosome 1 , 461 genetic ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
17 weitere Abschnitte werden nicht angezeigt.
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