Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 192
... studies of this myeloma cell line permitted accurate determination that approximately 47,000 molecules of light chain peptides were being synthesized per cell per second . Similarly , large amounts of this peptide were harvested from ...
... studies of this myeloma cell line permitted accurate determination that approximately 47,000 molecules of light chain peptides were being synthesized per cell per second . Similarly , large amounts of this peptide were harvested from ...
Seite 384
... STUDIES AND POLYGENIC INHERITANCE An interesting development in pharmacogenetics has been the use of twin studies in at- tempting to define genetic factors in drug metabolism . It is somewhat paradoxical that , as twin studies have ...
... STUDIES AND POLYGENIC INHERITANCE An interesting development in pharmacogenetics has been the use of twin studies in at- tempting to define genetic factors in drug metabolism . It is somewhat paradoxical that , as twin studies have ...
Seite 404
... studies with phenylbutazone , antipy- rine , bishydroxycoumarin , ethanol and halothane . Recently , Whittaker and Price Evans ( 1970 ) performed a family study to assess the genetic contribution to variability among individuals in ...
... studies with phenylbutazone , antipy- rine , bishydroxycoumarin , ethanol and halothane . Recently , Whittaker and Price Evans ( 1970 ) performed a family study to assess the genetic contribution to variability among individuals in ...
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