Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 72
Seite 80
... least acculturated and are similar to each other from a sociological point of view . Neither can be considered as unadulterated pa- leolithic or mesolithic hunters - gatherers , as at least during the last few centuries they have had ...
... least acculturated and are similar to each other from a sociological point of view . Neither can be considered as unadulterated pa- leolithic or mesolithic hunters - gatherers , as at least during the last few centuries they have had ...
Seite 87
... least not at polymorphic frequencies ) : ( 1 ) The delta hemoglobin chain mutant Flatbush . This had previously ... least one Pygmy camp , but usually to many . The analysis in the R.C.A. is much more complete and covers at least 1/3 of ...
... least not at polymorphic frequencies ) : ( 1 ) The delta hemoglobin chain mutant Flatbush . This had previously ... least one Pygmy camp , but usually to many . The analysis in the R.C.A. is much more complete and covers at least 1/3 of ...
Seite 302
... least anodal isozyme is much the most intense in staining activity and the others show progressively decreasing intensity with increasing anodal mobility . Simi- lar isozyme patterns were obtained using extracts of other tissues ...
... least anodal isozyme is much the most intense in staining activity and the others show progressively decreasing intensity with increasing anodal mobility . Simi- lar isozyme patterns were obtained using extracts of other tissues ...
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