Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 9
Seite 26
... amniocentesis to all pregnant women when and if data are obtained establishing more definitely the low frequency of immediate and / or long - term complications of amniocentesis . Note in Table 2 that for 1 of the 6 affected fetuses in ...
... amniocentesis to all pregnant women when and if data are obtained establishing more definitely the low frequency of immediate and / or long - term complications of amniocentesis . Note in Table 2 that for 1 of the 6 affected fetuses in ...
Seite 30
... amniocentesis in the early prenatal detection of genetic disorders . In : Intrauterine Diagnosis ; Birth Defects : Original Article Series , Vol . VII , No. 5 , pp . 5-9 . Editors : D. Bergsma and A. Motulsky . The National Foundation ...
... amniocentesis in the early prenatal detection of genetic disorders . In : Intrauterine Diagnosis ; Birth Defects : Original Article Series , Vol . VII , No. 5 , pp . 5-9 . Editors : D. Bergsma and A. Motulsky . The National Foundation ...
Seite 294
... amniocentesis of normal subjects in the second trimester of pregnancy ( Okada and O'Brien , 1969 ) . This suggested that the prenatal diagnosis of Tay- Sachs disease was possible . We then modified the fluorometric assay used for serum ...
... amniocentesis of normal subjects in the second trimester of pregnancy ( Okada and O'Brien , 1969 ) . This suggested that the prenatal diagnosis of Tay- Sachs disease was possible . We then modified the fluorometric assay used for serum ...
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