Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 275
... loci coding for enzyme structure . These findings imply that any single individual is likely to be heterozygous at many differ- ent gene loci , and it becomes of some interest to enquire what the average degree of such heterozygosity ...
... loci coding for enzyme structure . These findings imply that any single individual is likely to be heterozygous at many differ- ent gene loci , and it becomes of some interest to enquire what the average degree of such heterozygosity ...
Seite 300
... loci Isozymes may result due to the occurrence of two or more separate gene loci , each of which codes for a different polypeptide chain . Perhaps the best known example is lactate dehydrogenase where three distinct loci are concerned ...
... loci Isozymes may result due to the occurrence of two or more separate gene loci , each of which codes for a different polypeptide chain . Perhaps the best known example is lactate dehydrogenase where three distinct loci are concerned ...
Seite 447
... loci for Rh and elliptocytosis ( Chalmers and Lawler , 1953 ) and for Rh and 6 - PGD ( Weitkamp et al . , 1971b ) had been previously shown to be link- ed by pedigree analysis , but such methods had not yielded evidence suggestive of ...
... loci for Rh and elliptocytosis ( Chalmers and Lawler , 1953 ) and for Rh and 6 - PGD ( Weitkamp et al . , 1971b ) had been previously shown to be link- ed by pedigree analysis , but such methods had not yielded evidence suggestive of ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
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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