Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 181
... origin . Steel ( 1971 ) has re- examined the long D - like marker of chromosomes in cultured lines established from Burkitt's tumour and concludes that , in all cases , the chromosome is of different origin . The classic case of a ...
... origin . Steel ( 1971 ) has re- examined the long D - like marker of chromosomes in cultured lines established from Burkitt's tumour and concludes that , in all cases , the chromosome is of different origin . The classic case of a ...
Seite 236
... origin of this class of rearrangement will now be considered in more detail . ORIGIN OF EUPLOID STRUCTURAL REARRANGEMENTS OF THE AUTOSOMES A total of 26 babies ascertained in the neonatal surveys was found to have a euploid ...
... origin of this class of rearrangement will now be considered in more detail . ORIGIN OF EUPLOID STRUCTURAL REARRANGEMENTS OF THE AUTOSOMES A total of 26 babies ascertained in the neonatal surveys was found to have a euploid ...
Seite 237
... Origin of euploid rearrangements ( all data ) Rearrangement Total Both parents examined Both parents normal Affected parent Father Mother D / D 32 12 D / G 9 Reciprocal T. Inv . Total 41 20 7 89 24242 1 6 1 7 0 15 52025 6 18 6372∞ As ...
... Origin of euploid rearrangements ( all data ) Rearrangement Total Both parents examined Both parents normal Affected parent Father Mother D / D 32 12 D / G 9 Reciprocal T. Inv . Total 41 20 7 89 24242 1 6 1 7 0 15 52025 6 18 6372∞ As ...
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