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 40
... allele is present then the timing of H2 is determined by Int . However , if a matching Rec allele is present to prevent Int action , then the timing is taken over by the Tem gene further down on the X chromosome . Tem also has 2 alleles ...
... allele is present then the timing of H2 is determined by Int . However , if a matching Rec allele is present to prevent Int action , then the timing is taken over by the Tem gene further down on the X chromosome . Tem also has 2 alleles ...
Seite 298
... alleles occur with frequencies of between 1 and 10 to 15 % and in no case is there a single dominant allele at any of the loci . The overall level of heterozygosity is certainly much higher than that for any of the other known human ...
... alleles occur with frequencies of between 1 and 10 to 15 % and in no case is there a single dominant allele at any of the loci . The overall level of heterozygosity is certainly much higher than that for any of the other known human ...
Seite 321
... alleles each are known at the Ir - 1A and Ia - 3 loci ; and at least a couple of alleles are known at each of the remaining H - 2 loci . Most of these alleles have been defined by using inbred strains or congenic lines carrying wild ...
... alleles each are known at the Ir - 1A and Ia - 3 loci ; and at least a couple of alleles are known at each of the remaining H - 2 loci . Most of these alleles have been defined by using inbred strains or congenic lines carrying wild ...
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