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
... known human polymorphisms , including all the complex red cell blood groups ( Race and Sanger , 1975 ) and is well above the average frequency of heterozygotes per locus for man , which is about 15 % ( Harris , 1975 ) . Even if the HLA ...
... known human polymorphisms , including all the complex red cell blood groups ( Race and Sanger , 1975 ) and is well above the average frequency of heterozygotes per locus for man , which is about 15 % ( Harris , 1975 ) . Even if the HLA ...
Seite 321
... known for any mammalian locus ( Table 1 ) : over 20 alleles have been described at each of the two Class I loci ( H - 2K and 1-2D ) ; more than a dozen alleles each are known at the Ir - 1A and Ia - 3 loci ; and at least a couple of ...
... known for any mammalian locus ( Table 1 ) : over 20 alleles have been described at each of the two Class I loci ( H - 2K and 1-2D ) ; more than a dozen alleles each are known at the Ir - 1A and Ia - 3 loci ; and at least a couple of ...
Seite 406
... known about genetic predisposition to chemical carcinogens . Xeroderma pigmentosum and ataxia telangiectasia may both prove to be examples of such a predisposition . In xeroderma pigmentosum the defect in repair of damage to DNA extends ...
... known about genetic predisposition to chemical carcinogens . Xeroderma pigmentosum and ataxia telangiectasia may both prove to be examples of such a predisposition . In xeroderma pigmentosum the defect in repair of damage to DNA extends ...
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