Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 79
Seite 14
... test and the background ' static ' of false - positive tests , missed diagnosis and costs of the screening program ( and noise from the critics ! ) . To be more precise in this analogy , the ' signal ' is the index trait sought by the ...
... test and the background ' static ' of false - positive tests , missed diagnosis and costs of the screening program ( and noise from the critics ! ) . To be more precise in this analogy , the ' signal ' is the index trait sought by the ...
Seite 265
... tests are somehow culturally biased against children of low SES and in favor of middle - class white children . The tests are seen as seriously under- estimating the intelligence of low SES children . The fact that the IQ predicts ...
... tests are somehow culturally biased against children of low SES and in favor of middle - class white children . The tests are seen as seriously under- estimating the intelligence of low SES children . The fact that the IQ predicts ...
Seite 268
... tests , relative to those of middle SES , simply because Level I tests were less culturally biased than the IQ tests . This culture - bias hypothesis seems untenable in view of the fact that in the range of IQ above 100 , low SES ...
... tests , relative to those of middle SES , simply because Level I tests were less culturally biased than the IQ tests . This culture - bias hypothesis seems untenable in view of the fact that in the range of IQ above 100 , low SES ...
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