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 145
... addition to the three apoenzymes , two coenzymes are required to form three holoenzymes ; and there are two factors , one a protein which enhances hydroxylating activity , the other a lipid which stimulates purified hydroxylase activity ...
... addition to the three apoenzymes , two coenzymes are required to form three holoenzymes ; and there are two factors , one a protein which enhances hydroxylating activity , the other a lipid which stimulates purified hydroxylase activity ...
Seite 265
... addition , we have been able to get information bearing on the mode of action of mutant genes and on the frequency of occurrence of spontaneous and induced mutants in populations of cultured cells . Hence , the phenomena summarized in ...
... addition , we have been able to get information bearing on the mode of action of mutant genes and on the frequency of occurrence of spontaneous and induced mutants in populations of cultured cells . Hence , the phenomena summarized in ...
Seite 390
... addition , several observations concerning the incidence of the lactase phenotypes in racially mixed populations were interpreted in the light of the genetic hypothesis . This evidence is summarised in Tables 3 and 4 . A Finnish group ...
... addition , several observations concerning the incidence of the lactase phenotypes in racially mixed populations were interpreted in the light of the genetic hypothesis . This evidence is summarised in Tables 3 and 4 . A Finnish group ...
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