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
... frequency - dependent selection that is well known as a mechanism for giving rise to polymorphism ( Bodmer , 1972 ; Bodmer and Thomson , 1977 ) . There are , as might be expected , a number of substantial differences in gene frequencies ...
... frequency - dependent selection that is well known as a mechanism for giving rise to polymorphism ( Bodmer , 1972 ; Bodmer and Thomson , 1977 ) . There are , as might be expected , a number of substantial differences in gene frequencies ...
Seite 299
... frequency and the measure of linkage disequilibrium , D. When D is close to the haplotype frequency , then the contribution of the product of the gene frequencies to the haplotype frequency is small and D is near to its maximum possible ...
... frequency and the measure of linkage disequilibrium , D. When D is close to the haplotype frequency , then the contribution of the product of the gene frequencies to the haplotype frequency is small and D is near to its maximum possible ...
Seite 379
... frequency of about 1 in 2000 but the frequency of mildly affected persons is undoubtedly higher ( Stokes et al . , 1973 ) . The hereditary hyperlipidemias ( Motulsky , 1976 ) pose important nutritional questi- ons . There are three ...
... frequency of about 1 in 2000 but the frequency of mildly affected persons is undoubtedly higher ( Stokes et al . , 1973 ) . The hereditary hyperlipidemias ( Motulsky , 1976 ) pose important nutritional questi- ons . There are three ...
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