Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 29
... prenatal diagnosis of hemophilia is now possible with a high degree of accuracy for women who are heterozygous at the dehydro- genase locus and who have had one son with hemophilia or are known to be carriers of hemo- philia from other ...
... prenatal diagnosis of hemophilia is now possible with a high degree of accuracy for women who are heterozygous at the dehydro- genase locus and who have had one son with hemophilia or are known to be carriers of hemo- philia from other ...
Seite 297
... prenatal diagnosis and selective termination . Thus , the program appears to be economically feasible for North American Jews . However , due to the low gene frequency among non - Jews , and the very large population size , it is not ...
... prenatal diagnosis and selective termination . Thus , the program appears to be economically feasible for North American Jews . However , due to the low gene frequency among non - Jews , and the very large population size , it is not ...
Seite 498
... prenatal diagnosis , 25 , 26 sex linked disease prenatal diagnosis , 25 , 26 Shope virus genetic engineering , 37 , 38 sickle cell anemia linkage data use , counseling and prenatal diagnosis , 455 prenatal diagnosis , 29 Pygmies and ...
... prenatal diagnosis , 25 , 26 sex linked disease prenatal diagnosis , 25 , 26 Shope virus genetic engineering , 37 , 38 sickle cell anemia linkage data use , counseling and prenatal diagnosis , 455 prenatal diagnosis , 29 Pygmies and ...
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