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 143
... polymorphism among members of the normal population . We realize now , of course , that this polymorphism in the mutant genotype is highly pertinent to the diagnosis and interpretation of an inborn error of metabolism , and to the ...
... polymorphism among members of the normal population . We realize now , of course , that this polymorphism in the mutant genotype is highly pertinent to the diagnosis and interpretation of an inborn error of metabolism , and to the ...
Seite 298
... polymorphism would occur in the absence of some distinguishing feature of the HLA system . One possible explanation for the relatively high level of polymorphism of HLA loci is that their functions may be such as to tend to give a ...
... polymorphism would occur in the absence of some distinguishing feature of the HLA system . One possible explanation for the relatively high level of polymorphism of HLA loci is that their functions may be such as to tend to give a ...
Seite 321
... polymorphism unless it can be established that all these alleles occur with appreciable frequencies in wild mouse populations . Unfortunately , until recently , data on H - 2 gene frequencies in wild mice has not been available , and it ...
... polymorphism unless it can be established that all these alleles occur with appreciable frequencies in wild mouse populations . Unfortunately , until recently , data on H - 2 gene frequencies in wild mice has not been available , and it ...
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