Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 232
... frequency with which chromosome aberrations were found in spontaneous abortions . However , very little was known about the frequency of individuals with abnormalities of the Y chromosome , or of the effects of such abnormalities on the ...
... frequency with which chromosome aberrations were found in spontaneous abortions . However , very little was known about the frequency of individuals with abnormalities of the Y chromosome , or of the effects of such abnormalities on the ...
Seite 281
... frequencies in the same populations . In most populations PIM has a frequency of 0.85-0.99 . The high Pis frequency in Iberians is remarkable , and is supported by similar results among Latin Americans and people living in southern ...
... frequencies in the same populations . In most populations PIM has a frequency of 0.85-0.99 . The high Pis frequency in Iberians is remarkable , and is supported by similar results among Latin Americans and people living in southern ...
Seite 448
... frequency . Several approximate formulae have been used to describe the relationship between map interval and recombination fraction ( cf. Renwick , 1969 ) , but whichever is used , the relative map distance is generally not ...
... frequency . Several approximate formulae have been used to describe the relationship between map interval and recombination fraction ( cf. Renwick , 1969 ) , but whichever is used , the relative map distance is generally not ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
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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