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 41
... important is in the possible role that quantitative variation in enzyme levels may play in determining disease susceptibility . What we do know is that quantitative polymorphisms are reasonably common in both man and animal systems ...
... important is in the possible role that quantitative variation in enzyme levels may play in determining disease susceptibility . What we do know is that quantitative polymorphisms are reasonably common in both man and animal systems ...
Seite 232
... important . In addition , the exposure of our populations to increased levels of radiation and chemical mutagens gives this problem an important practical aspect . Studies TABLE 5 Key problems in human population genetics 1. What is the ...
... important . In addition , the exposure of our populations to increased levels of radiation and chemical mutagens gives this problem an important practical aspect . Studies TABLE 5 Key problems in human population genetics 1. What is the ...
Seite 251
... important . Where drift alone is important f will vary proportionally to time if small , but if it is large a function log ( 1 - f ) is more relevant : where variable selection is operating then √f will be proportional to time ...
... important . Where drift alone is important f will vary proportionally to time if small , but if it is large a function log ( 1 - f ) is more relevant : where variable selection is operating then √f will be proportional to time ...
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