Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 232
... techniques ( Sumner et al . , 1971 ) . As such techniques , as applied to human chromosomes , are scarcely a year old we are only just beginning to ex- ploit the advantages made available by this increase in precision . In the present ...
... techniques ( Sumner et al . , 1971 ) . As such techniques , as applied to human chromosomes , are scarcely a year old we are only just beginning to ex- ploit the advantages made available by this increase in precision . In the present ...
Seite 241
... techniques , or by the use of fluorescent or anneal- ing techniques , we now have available under the light microscope direct evidence of an enormous wealth of genetic variation . The origin and significance of this variation in terms ...
... techniques , or by the use of fluorescent or anneal- ing techniques , we now have available under the light microscope direct evidence of an enormous wealth of genetic variation . The origin and significance of this variation in terms ...
Seite 365
... techniques , 2. genetic markers which can be detected in cells in culture , and 3. methods for genetic analysis using cells in culture . The techniques of cell culture are now well developed and many cell lines can be cloned with high ...
... techniques , 2. genetic markers which can be detected in cells in culture , and 3. methods for genetic analysis using cells in culture . The techniques of cell culture are now well developed and many cell lines can be cloned with high ...
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