Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 243
... Mental Retardation , Staten Island , N. Y. , U.S.A. Introductory remarks Genetic problems of mental retardation are as old as human genetics itself . During the past decade or so we have witnessed a truly extraordinary development of ...
... Mental Retardation , Staten Island , N. Y. , U.S.A. Introductory remarks Genetic problems of mental retardation are as old as human genetics itself . During the past decade or so we have witnessed a truly extraordinary development of ...
Seite 255
... mental illness , and there was nothing signifi- cant in the history of the third . Of the six twins from the discordant group who had an IQ below 50 , one with an IQ of 38 had grand mal seizures from age 4 months to 5 years and a ...
... mental illness , and there was nothing signifi- cant in the history of the third . Of the six twins from the discordant group who had an IQ below 50 , one with an IQ of 38 had grand mal seizures from age 4 months to 5 years and a ...
Seite 256
... mental retardation Concordant twins One twin Primary apnea Pneumococcal meningitis at age 2 months Congenital heart disease Sickle cell trait Mother Severe anemia during ... Mental retardation Mental illness 256 N. C. MYRIANTHOPOULOS ET AL .
... mental retardation Concordant twins One twin Primary apnea Pneumococcal meningitis at age 2 months Congenital heart disease Sickle cell trait Mother Severe anemia during ... Mental retardation Mental illness 256 N. C. MYRIANTHOPOULOS ET AL .
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