Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 276
... variants that may actually occur can be detected electrophoretically . So it is probable that the average heterozygosity per locus for alleles resulting in structural differences of enzymes is about three times that calculated on the ...
... variants that may actually occur can be detected electrophoretically . So it is probable that the average heterozygosity per locus for alleles resulting in structural differences of enzymes is about three times that calculated on the ...
Seite 277
... variant protein is present in a sufficiently high concentration . Some variants have a normal mobility on agarose gels , but have clearly in- creased or decreased mobility on acid starch gel electrophoresis . The presence of variants ...
... variant protein is present in a sufficiently high concentration . Some variants have a normal mobility on agarose gels , but have clearly in- creased or decreased mobility on acid starch gel electrophoresis . The presence of variants ...
Seite 304
... variant NP isozyme patterns were discovered . These variants are shown in Figure 4 together with the usual pattern ( NP1 ) which has been discussed earlier . Family studies carried out using red cell samples showed that these complex ...
... variant NP isozyme patterns were discovered . These variants are shown in Figure 4 together with the usual pattern ( NP1 ) which has been discussed earlier . Family studies carried out using red cell samples showed that these complex ...
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