Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 26
Seite 12
... Screening for genetic variation may serve one or more purposes . There is still a basic need for information about the frequency , natural history and inheritance of much genetic disease ; some types of screening can help supply this ...
... Screening for genetic variation may serve one or more purposes . There is still a basic need for information about the frequency , natural history and inheritance of much genetic disease ; some types of screening can help supply this ...
Seite 14
... screening except to note that new methods for staining human chro- mosomes have already recharged cytogenetic research and the field has gained renewed momentum . Screening for the disease itself ( level IV ) is not often desirable ...
... screening except to note that new methods for staining human chro- mosomes have already recharged cytogenetic research and the field has gained renewed momentum . Screening for the disease itself ( level IV ) is not often desirable ...
Seite 387
... screening could be quite useful in the interpretation of anemias . Screening for pseudocholinesterase abnormality is usually not done , yet 1/3000 Caucasians will have pro- longed apnea when given suxamethonium . With good ...
... screening could be quite useful in the interpretation of anemias . Screening for pseudocholinesterase abnormality is usually not done , yet 1/3000 Caucasians will have pro- longed apnea when given suxamethonium . With good ...
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