Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 5
... malformations like those caused by thalidomide only before the 40th or only after the 45th day are seen in the thrombocytopenia - radius aplasia syndrome . One might suppose , therefore , that the normal alleles of the genes underlying ...
... malformations like those caused by thalidomide only before the 40th or only after the 45th day are seen in the thrombocytopenia - radius aplasia syndrome . One might suppose , therefore , that the normal alleles of the genes underlying ...
Seite 8
Jean de Grouchy, Francis John Govier Ebling, I. W. Henderson. the common congenital malformations such as spina ... malformation in any random pregnancy , and secondly to explain the prognosis for the child if it should be affected . It ...
Jean de Grouchy, Francis John Govier Ebling, I. W. Henderson. the common congenital malformations such as spina ... malformation in any random pregnancy , and secondly to explain the prognosis for the child if it should be affected . It ...
Seite 57
... malformations following low doses of radiation to trout sperm . Radiat . Res . , 49 , 155 . MULLER , M. J. ( 1950 ) : Our load of mutations . Amer . J. hum . Genet . , 2 , 111 . NEWCOMBE , H. B. ( 1964 ) : Panel discussion of the ...
... malformations following low doses of radiation to trout sperm . Radiat . Res . , 49 , 155 . MULLER , M. J. ( 1950 ) : Our load of mutations . Amer . J. hum . Genet . , 2 , 111 . NEWCOMBE , H. B. ( 1964 ) : Panel discussion of the ...
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