Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 105
... indicate major areas drained by the rivers whose names are given . The 7 names at the bottom ( with letter designations ) indicate the sites of the 7 villages studied . Each name in the schema itself indicates the site of a village ...
... indicate major areas drained by the rivers whose names are given . The 7 names at the bottom ( with letter designations ) indicate the sites of the 7 villages studied . Each name in the schema itself indicates the site of a village ...
Seite 417
... indicate that malignant hyperthermia with rigidity occurs on the basis of a defect in skeletal muscle . The first evidence came from the clinical observation that rigidity did not develop in limb when a tourniquet prevented its being ...
... indicate that malignant hyperthermia with rigidity occurs on the basis of a defect in skeletal muscle . The first evidence came from the clinical observation that rigidity did not develop in limb when a tourniquet prevented its being ...
Seite 434
... indicate a dominant character transmitted as a single gene effect in 4 generations of the family . Male - to - male transmission of the resistance to 4 sons ( III - 26 , III - 27 , III - 29 and III - 30 ) from 2 fathers ( II - 22 and II ...
... indicate a dominant character transmitted as a single gene effect in 4 generations of the family . Male - to - male transmission of the resistance to 4 sons ( III - 26 , III - 27 , III - 29 and III - 30 ) from 2 fathers ( II - 22 and II ...
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