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 39
... appears . In some strains H2 appears virtually at birth and in others it does not appear until 4 days later . Several crosses and inbred lines were established in developing a model . Three temporal genes are thought to participate in ...
... appears . In some strains H2 appears virtually at birth and in others it does not appear until 4 days later . Several crosses and inbred lines were established in developing a model . Three temporal genes are thought to participate in ...
Seite 66
... appears to be defective , apparently one which concerns the removal of interstrand crosslinks and the restoration thereafter of the continuity of the DNA . Extracts from some FA cell lines also exhibit a lower than normal capacity to ...
... appears to be defective , apparently one which concerns the removal of interstrand crosslinks and the restoration thereafter of the continuity of the DNA . Extracts from some FA cell lines also exhibit a lower than normal capacity to ...
Seite 291
... appears the most likely explanation for activation . While there are reports that extinction of hemoglobin production in Friend cell hybrids is accompanied by absence of cytoplasmic mRNA for globin ( Deisseroth et al . , 1976 ) , direct ...
... appears the most likely explanation for activation . While there are reports that extinction of hemoglobin production in Friend cell hybrids is accompanied by absence of cytoplasmic mRNA for globin ( Deisseroth et al . , 1976 ) , direct ...
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