Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 386
... autosomal dominant type II hypercholesterolemia ( Levy and Langer , 1971 ) and others with a more poorly defined separate genetic disorder associated with elevation in both triglycerides and cholesterol . Other diseases such as ...
... autosomal dominant type II hypercholesterolemia ( Levy and Langer , 1971 ) and others with a more poorly defined separate genetic disorder associated with elevation in both triglycerides and cholesterol . Other diseases such as ...
Seite 392
... Autosomal recessive Hydrogen peroxide Autosomal recessive Pseudocholinesterase in plasma Autosomal recessive ? Mixed function oxidase in liver microsomes that parahydroxylates diphenylhydantoin Autosomal dominant ? Altered receptor or ...
... Autosomal recessive Hydrogen peroxide Autosomal recessive Pseudocholinesterase in plasma Autosomal recessive ? Mixed function oxidase in liver microsomes that parahydroxylates diphenylhydantoin Autosomal dominant ? Altered receptor or ...
Seite 487
... autosomal aberration aneuploidy , 237 , 238 frequency , newborn , 233 , 235 , 236 mutation rate , 237 , 238 origin , 237 , 238 segregation , 238-240 autosomal dominant heritance Lp system , 345 , 347 , 352 malignant hyperthermia , 415 ...
... autosomal aberration aneuploidy , 237 , 238 frequency , newborn , 233 , 235 , 236 mutation rate , 237 , 238 origin , 237 , 238 segregation , 238-240 autosomal dominant heritance Lp system , 345 , 347 , 352 malignant hyperthermia , 415 ...
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