Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
Im Buch
Ergebnisse 1-3 von 45
Seite 398
... plasma of 3 sets of identical twins ( left ) and 3 sets of frater- nal twins ( right ) . The log of the phenylbutazone concentration in 2 ml of plasma is shown at intervals after a single oral dose of 6 mg / kg . ( Reproduced from ...
... plasma of 3 sets of identical twins ( left ) and 3 sets of frater- nal twins ( right ) . The log of the phenylbutazone concentration in 2 ml of plasma is shown at intervals after a single oral dose of 6 mg / kg . ( Reproduced from ...
Seite 400
... plasma of 3 sets of identical twins ( left ) and 3 sets of fraternal twins ( right ) . The log of the bishydroxycoumarin concentration in 2 ml of plasma is shown at intervals after a single oral dose of 4 mg / kg . ( Reproduced from ...
... plasma of 3 sets of identical twins ( left ) and 3 sets of fraternal twins ( right ) . The log of the bishydroxycoumarin concentration in 2 ml of plasma is shown at intervals after a single oral dose of 4 mg / kg . ( Reproduced from ...
Seite 409
... plasma anti- pyrine or bishydroxycoumarin half - life , determined after a single oral dose at 9:00 A.M. of antipyrine ( 18 mg / kg ) or bishydroxycoumarin ( 4 mg / kg ) . Afterward , each volunteer received either nortriptyline ( 0.2 ...
... plasma anti- pyrine or bishydroxycoumarin half - life , determined after a single oral dose at 9:00 A.M. of antipyrine ( 18 mg / kg ) or bishydroxycoumarin ( 4 mg / kg ) . Afterward , each volunteer received either nortriptyline ( 0.2 ...
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