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 65
... demonstrated to be the case for one of them when decreased ' unscheduled DNA synthesis ' was found in UV - treated XP cells ( Cleaver and Bootsma , 1975 ) . DNA repair mechanisms are being studied intensively in XP and the remaining ...
... demonstrated to be the case for one of them when decreased ' unscheduled DNA synthesis ' was found in UV - treated XP cells ( Cleaver and Bootsma , 1975 ) . DNA repair mechanisms are being studied intensively in XP and the remaining ...
Seite 367
... demonstrated that these environmental agents can cause cancer via effects upon DNA , that is , broadly speaking , via somatic mutation . But some chemical carcinogens seemed for a long time not to act as mutagens because they were not ...
... demonstrated that these environmental agents can cause cancer via effects upon DNA , that is , broadly speaking , via somatic mutation . But some chemical carcinogens seemed for a long time not to act as mutagens because they were not ...
Seite 380
... demonstrated in the newborn period ( Wolff , 1972 ) . The genetic determinants of this phenomenon have not been studied . However , most Orientals have an atypical alcohol dehydrogenase in their livers ( Stamatayanopoulos et al . , 1975 ) ...
... demonstrated in the newborn period ( Wolff , 1972 ) . The genetic determinants of this phenomenon have not been studied . However , most Orientals have an atypical alcohol dehydrogenase in their livers ( Stamatayanopoulos et al . , 1975 ) ...
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