Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 61
... shown that translocation frequencies in guinea - pig and rabbit spermatocytes after spermatogonial X - ray doses of 300 rads or less were not greatly different from those in the mouse , but declined sharply at higher doses . Results so ...
... shown that translocation frequencies in guinea - pig and rabbit spermatocytes after spermatogonial X - ray doses of 300 rads or less were not greatly different from those in the mouse , but declined sharply at higher doses . Results so ...
Seite 283
... shown that this is the case for sea urchins . Kueppers ( 19716 ) has shown that rabbit sperm contains a protease which reacts with the protein corresponding to a - 1 - at in rabbit serum . It has been shown by Hagström ( 1961 ) and ...
... shown that this is the case for sea urchins . Kueppers ( 19716 ) has shown that rabbit sperm contains a protease which reacts with the protein corresponding to a - 1 - at in rabbit serum . It has been shown by Hagström ( 1961 ) and ...
Seite 433
... shown here . On the abscissa are the blood levels of warfarin at 48 hours with the 99 % confidence limits for normal subjects shown by the dotted lines , and on the ordinate the prothrombin activity at 0 hours ( the circles ) and 48 ...
... shown here . On the abscissa are the blood levels of warfarin at 48 hours with the 99 % confidence limits for normal subjects shown by the dotted lines , and on the ordinate the prothrombin activity at 0 hours ( the circles ) and 48 ...
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