Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 94
... problem of daily food . By contrast , Pygmies have continued to live on the products of the forest , to which they have learned to adapt so well . They have no problems with the limited seasonal variation . They learned to establish and ...
... problem of daily food . By contrast , Pygmies have continued to live on the products of the forest , to which they have learned to adapt so well . They have no problems with the limited seasonal variation . They learned to establish and ...
Seite 357
... problems encountered are inherent in any work with such lipid - protein compounds . The lability of the antigens together with the immunological problems could presumably lead to irregularity in the manifestation even of a system ...
... problems encountered are inherent in any work with such lipid - protein compounds . The lability of the antigens together with the immunological problems could presumably lead to irregularity in the manifestation even of a system ...
Seite 479
... problems of western society , and rather lately it has been promoted as a means for killing deformed babies and useless old men . CONCLUSION - FUTURE GENERATIONS : FAITH OF POPE PAUL VI Turning the pages of history , and focusing upon ...
... problems of western society , and rather lately it has been promoted as a means for killing deformed babies and useless old men . CONCLUSION - FUTURE GENERATIONS : FAITH OF POPE PAUL VI Turning the pages of history , and focusing upon ...
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