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 19
... estimates of mutation rates is untenable because of the inability at present to estimate for ' recessive ' traits ... estimates for man , based on some 17 phenotypes . These estimates range from 104 to 10-7 / gene / generation , with an ...
... estimates of mutation rates is untenable because of the inability at present to estimate for ' recessive ' traits ... estimates for man , based on some 17 phenotypes . These estimates range from 104 to 10-7 / gene / generation , with an ...
Seite 27
... estimate Several years ago , I applied the Kimura - Ohta formula to data on rare protein variants in Amerindians still ... estimates of human mutation rates at the protein level , those of Motulsky ( 1968 ) and Kimura and Ohta ( 1973 ) ...
... estimate Several years ago , I applied the Kimura - Ohta formula to data on rare protein variants in Amerindians still ... estimates of human mutation rates at the protein level , those of Motulsky ( 1968 ) and Kimura and Ohta ( 1973 ) ...
Seite 28
... estimates in line . Although ultimately these estimates may be of only historical interest , they are important for the methodology they introduce . An alternative , direct approach to estimating mutation rates is illustrated by the ...
... estimates in line . Although ultimately these estimates may be of only historical interest , they are important for the methodology they introduce . An alternative , direct approach to estimating mutation rates is illustrated by the ...
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