Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 250
... twins and singletons by race Twins Singletons Difference in means Mean SD Mean SD White Verbal scale 96.0 14.3 100.0 13.7 -4.0 Performance scale 101.5 13.4 103.8 14.4 -2.3 Full - scale IQ 96.9 14.8 101.9 13.5 -5.0 Negro Verbal scale ...
... twins and singletons by race Twins Singletons Difference in means Mean SD Mean SD White Verbal scale 96.0 14.3 100.0 13.7 -4.0 Performance scale 101.5 13.4 103.8 14.4 -2.3 Full - scale IQ 96.9 14.8 101.9 13.5 -5.0 Negro Verbal scale ...
Seite 254
... twins come from families of lower socioecono- mic background than that of twins in general . The drop in socioeconomic index is mainly due to the preponderance and contribution of Negro twin pairs . When examined by race , the mean ...
... twins come from families of lower socioecono- mic background than that of twins in general . The drop in socioeconomic index is mainly due to the preponderance and contribution of Negro twin pairs . When examined by race , the mean ...
Seite 255
... twins from the concordant group who had an IQ below 50 , one had pneumococcal meningitis at age 23 months , the mother of the second had a history of convulsive disorder and mental illness , and there was nothing signifi- cant in the ...
... twins from the concordant group who had an IQ below 50 , one had pneumococcal meningitis at age 23 months , the mother of the second had a history of convulsive disorder and mental illness , and there was nothing signifi- cant in the ...
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