Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 39
Seite 52
... alleles . And even then , the extent of the increase in variation would be further restricted to situa- tions in which the rare alleles that do exist have effects which are different in direction and magnitude from those of the common ...
... alleles . And even then , the extent of the increase in variation would be further restricted to situa- tions in which the rare alleles that do exist have effects which are different in direction and magnitude from those of the common ...
Seite 273
... alleles may in principle be generated from a single gene by separate mutational events . For example , from a gene containing a sequence of DNA say 900 bases long and coding for a polypeptide of 300 aminoacids , 2,700 different alleles ...
... alleles may in principle be generated from a single gene by separate mutational events . For example , from a gene containing a sequence of DNA say 900 bases long and coding for a polypeptide of 300 aminoacids , 2,700 different alleles ...
Seite 275
... alleles occur in human populations . The majority of those alleles of course are rare , and many appear to have frequencies of the order of 1 in 10,000 or less . But some are relatively common and give rise to the well known ...
... alleles occur in human populations . The majority of those alleles of course are rare , and many appear to have frequencies of the order of 1 in 10,000 or less . But some are relatively common and give rise to the well known ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
17 weitere Abschnitte werden nicht angezeigt.
Häufige Begriffe und Wortgruppen
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