Génétique HumaineJean de Grouchy, Francis John Govier Ebling, I. W. Henderson Excerpta Medica, 1972 - 499 Seiten |
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Seite 188
... lines for genetic and clinical studies * The ease with which permanent lymphoid cell lines can be established from the peripheral blood , both from patients with various diseases and congenital abnormalities and from nor- mal persons ...
... lines for genetic and clinical studies * The ease with which permanent lymphoid cell lines can be established from the peripheral blood , both from patients with various diseases and congenital abnormalities and from nor- mal persons ...
Seite 189
... lines from patients with myelogenous leukemia , other cancerous diseases , and normal persons . It is easiest to estab- lish lymphoid cell lines from children and young adults with infectious mononucleosis and other viral diseases that ...
... lines from patients with myelogenous leukemia , other cancerous diseases , and normal persons . It is easiest to estab- lish lymphoid cell lines from children and young adults with infectious mononucleosis and other viral diseases that ...
Seite 190
... lines contain herpes - like virus ( EB virus ) and , in an additional number of cell lines , EB virus - associated antigens can be identified by fluorescent staining . The effects of EB virus on the genetic constitution of the lymphoid ...
... lines contain herpes - like virus ( EB virus ) and , in an additional number of cell lines , EB virus - associated antigens can be identified by fluorescent staining . The effects of EB virus on the genetic constitution of the lymphoid ...
Inhalt
Clinical geneticsGénétique clinique | 25 |
Radiation geneticsRadiations ionisantes | 38 |
Données récentes sur les taux de mutations radioinduites chez | 67 |
Urheberrecht | |
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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