Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 181
... reported on numerous occasions , but again the occurrence of the same abnormal chro- mosome in a number of cases of the same tumour is rare . Examples have been described in testicular tumours ( Martineau , 1967 ) and in Burkitt's ...
... reported on numerous occasions , but again the occurrence of the same abnormal chro- mosome in a number of cases of the same tumour is rare . Examples have been described in testicular tumours ( Martineau , 1967 ) and in Burkitt's ...
Seite 223
... reported and cases with lines of different autosomal trisomies are on record . Regrettably , in most cases chimerism has not been ruled out . Nevertheless , in occasional reports such attempts have been unsuccess- ful and one has to ...
... reported and cases with lines of different autosomal trisomies are on record . Regrettably , in most cases chimerism has not been ruled out . Nevertheless , in occasional reports such attempts have been unsuccess- ful and one has to ...
Seite 359
... reported by Simons et al . ( 1970 ) and on papain solubilized HL - A and H - 2 alloantigens published by Mann's group ( Mann et al . , 1970 ) we have conducted the first comparison of the amino acid composition of serum lipoproteins and ...
... reported by Simons et al . ( 1970 ) and on papain solubilized HL - A and H - 2 alloantigens published by Mann's group ( Mann et al . , 1970 ) we have conducted the first comparison of the amino acid composition of serum lipoproteins and ...
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