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 15
... estimated the proportion of the phenotypic variance that is genetic , i.e. the heritability . The methodological problems of heritability studies are well known . To put the matter succinctly , an estimate of genetic variance that is ...
... estimated the proportion of the phenotypic variance that is genetic , i.e. the heritability . The methodological problems of heritability studies are well known . To put the matter succinctly , an estimate of genetic variance that is ...
Seite 27
... estimate Several years ago , I applied the Kimura - Ohta formula to data on rare protein variants in Amerindians still maintaining their tribal integrity ( Neel , 1973 ) . The necessary estimate of 7 was obtained from a Monte Carlo ...
... estimate Several years ago , I applied the Kimura - Ohta formula to data on rare protein variants in Amerindians still maintaining their tribal integrity ( Neel , 1973 ) . The necessary estimate of 7 was obtained from a Monte Carlo ...
Seite 28
... estimate , based on the extensive screenings for hemoglobin variants carried out by Japanese investigators , was for the total mutation rate for the a and ß structural genes ( coding for 287 amino acids ) . The frequency of ...
... estimate , based on the extensive screenings for hemoglobin variants carried out by Japanese investigators , was for the total mutation rate for the a and ß structural genes ( coding for 287 amino acids ) . The frequency of ...
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