Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 33
... single mutations will cause in the pattern , or developmental program , for the production of individual proteins . Such programs can be defined experimentally by measuring enzyme activities in each tissue as development progresses ...
... single mutations will cause in the pattern , or developmental program , for the production of individual proteins . Such programs can be defined experimentally by measuring enzyme activities in each tissue as development progresses ...
Seite 309
... single foreign haplotype ( Wilson et al . , 1968 ) . Under analogous conditions in man the response to an array of gene products coded for by one foreign haplotype can be considered in two parts : one being to gene products of the HLA ...
... single foreign haplotype ( Wilson et al . , 1968 ) . Under analogous conditions in man the response to an array of gene products coded for by one foreign haplotype can be considered in two parts : one being to gene products of the HLA ...
Seite 310
... single cell - sensitized and from single cell - sensitized to pool- sensitized . ** In this comparison not all responders were sensitized to the pool so the number in this group is smaller . haplotypes ( Table 1 ) . It was possible that ...
... single cell - sensitized and from single cell - sensitized to pool- sensitized . ** In this comparison not all responders were sensitized to the pool so the number in this group is smaller . haplotypes ( Table 1 ) . It was possible that ...
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