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
... considered analogous to the concept of 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 ...
... considered analogous to the concept of 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 ...
Seite 191
... considered . In these cases 22 % of mosaics were confirmed on the fetus or baby , a relatively high rate , if these cases were to be misdiagnosed . The origin of mosaicism in amniotic fluid cultures is not clear , except in cases of ...
... considered . In these cases 22 % of mosaics were confirmed on the fetus or baby , a relatively high rate , if these cases were to be misdiagnosed . The origin of mosaicism in amniotic fluid cultures is not clear , except in cases of ...
Seite 309
... considered in two parts : one being to gene products of the HLA - D locus and the other to gene products of other loci termed non - HLA - D loci . Products of the HLA - D locus have hitherto been identified by the so - called negative ...
... considered in two parts : one being to gene products of the HLA - D locus and the other to gene products of other loci termed non - HLA - D loci . Products of the HLA - D locus have hitherto been identified by the so - called negative ...
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