Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 82
Seite 268
... Level I 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 ...
... Level I 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 ...
Seite 270
... Level I ability , on the other hand , is more or less equally advantageous in all cultures and walks of life and would therefore become less differentiated than Level II among various population groups . PHYSIOLOGICAL BASIS OF LEVEL 1 ...
... Level I ability , on the other hand , is more or less equally advantageous in all cultures and walks of life and would therefore become less differentiated than Level II among various population groups . PHYSIOLOGICAL BASIS OF LEVEL 1 ...
Seite 271
... Level I ability but are often quite far below average in Level II . Such children might benefit educationally from instructional methods which make the acquisition of scholastic skills less dependent upon Level II abilities and more ...
... Level I ability but are often quite far below average in Level II . Such children might benefit educationally from instructional methods which make the acquisition of scholastic skills less dependent upon Level II abilities and more ...
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