Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 83
Seite 117
... individuals are dis- tributed more or less discontinuously to form numerous colonies , and are exchanged mainly between adjacent or nearby groups . Isolation may thus be viewed as a function of the dis- tance between colonies . Wright ...
... individuals are dis- tributed more or less discontinuously to form numerous colonies , and are exchanged mainly between adjacent or nearby groups . Isolation may thus be viewed as a function of the dis- tance between colonies . Wright ...
Seite 396
... individuals in the nature of their physiologic or toxic receptor sites for drugs , but rather from differences among individuals in rates of drug clearance from the blood . Uniformity in the type of DPH toxicity produced by a given ...
... individuals in the nature of their physiologic or toxic receptor sites for drugs , but rather from differences among individuals in rates of drug clearance from the blood . Uniformity in the type of DPH toxicity produced by a given ...
Seite 412
... individuals in rates of drug clearance suggest that the extremes of toxicity and undertreatment can best be avoided if drug concentrations in blood serve as guides to adjust dosage . Studies establishing signifi- cantly less intratwin ...
... individuals in rates of drug clearance suggest that the extremes of toxicity and undertreatment can best be avoided if drug concentrations in blood serve as guides to adjust dosage . Studies establishing signifi- cantly less intratwin ...
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