Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
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Seite 287
... specific proteins . Thus , a stable dedifferentiated variant of the rat hepatoma line , which fails to produce all of the liver - specific proteins ( Deschatrette and Weiss , 1974 ) , has acquired the capacity to extinguish each of the ...
... specific proteins . Thus , a stable dedifferentiated variant of the rat hepatoma line , which fails to produce all of the liver - specific proteins ( Deschatrette and Weiss , 1974 ) , has acquired the capacity to extinguish each of the ...
Seite 291
... specific functions . The phenomena of extinction and of activation show that the production of tissue - specific proteins can be regulated by diffusible substances whose activity is trans - dominant and whose final effect may be ...
... specific functions . The phenomena of extinction and of activation show that the production of tissue - specific proteins can be regulated by diffusible substances whose activity is trans - dominant and whose final effect may be ...
Seite 362
... specific abnormality of chromosome 14 in particular in Burkitt's tumour there is a t ( 8 ; 14 ) translocation in many cases ( Zech et al . , 1976 ) . It is now apparent that in the myeloproliferative disorders the aneuploidy which has ...
... specific abnormality of chromosome 14 in particular in Burkitt's tumour there is a t ( 8 ; 14 ) translocation in many cases ( Zech et al . , 1976 ) . It is now apparent that in the myeloproliferative disorders the aneuploidy which has ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel