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 298
... occur with frequencies of between 1 and 10 to 15 % and in no case is there a single dominant allele at any of the loci . The overall level of heterozygosity is certainly much higher than that for any of the other known human ...
... occur with frequencies of between 1 and 10 to 15 % and in no case is there a single dominant allele at any of the loci . The overall level of heterozygosity is certainly much higher than that for any of the other known human ...
Seite 363
... occur there must be either specific aberration induction or selection for specific karyotypes . One attempt to ... occur in all individuals as a result of exposure to environmental agents . They will occur more Induced chromosome ...
... occur there must be either specific aberration induction or selection for specific karyotypes . One attempt to ... occur in all individuals as a result of exposure to environmental agents . They will occur more Induced chromosome ...
Seite 405
... occur particularly in areas exposed to sunlight and are also induced by ionizing radiation , as for the treatment of medulloblastoma , when it occurs in patients with the syndrome . However , there is no defect in DNA repair . An ...
... occur particularly in areas exposed to sunlight and are also induced by ionizing radiation , as for the treatment of medulloblastoma , when it occurs in patients with the syndrome . However , there is no defect in DNA repair . An ...
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