Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 65
Seite 11
... increased steadily in the past two decades ( Fig . 2 ) because of available technology , mass screening and ... increased local interest in case finding . The increased demand on care facilities is a direct legacy of increased activity ...
... increased steadily in the past two decades ( Fig . 2 ) because of available technology , mass screening and ... increased local interest in case finding . The increased demand on care facilities is a direct legacy of increased activity ...
Seite 435
... increased metabolic transformation , excretion , or volume of distribution of the drug ; 3. increased production of clotting factors dependent on vitamin K ; 4. prolonged biologic half - life of clotting factors dependent on vitamin K ...
... increased metabolic transformation , excretion , or volume of distribution of the drug ; 3. increased production of clotting factors dependent on vitamin K ; 4. prolonged biologic half - life of clotting factors dependent on vitamin K ...
Seite 451
... increased recombination with advanced pa- rental age ( P < 0.01 ) . In addition , in only 3 of the 8 families ... increased parental age there is significantly increased recom- bination in males ( p < 0.05 ) and possibly decreased ...
... increased recombination with advanced pa- rental age ( P < 0.01 ) . In addition , in only 3 of the 8 families ... increased parental age there is significantly increased recom- bination in males ( p < 0.05 ) and possibly decreased ...
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