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 21
... protein structure Technical aspects The feasibility of carrying the study of mutation rates to the protein level depends entirely on recent technical developments . For the immediate future , the backbone of any study involving the ...
... protein structure Technical aspects The feasibility of carrying the study of mutation rates to the protein level depends entirely on recent technical developments . For the immediate future , the backbone of any study involving the ...
Seite 23
... protein variants through mutation and their loss because of the operation of selective forces or by chance . If one is willing to make the assumption that the protein variants under study are essentially neutral with reference to their ...
... protein variants through mutation and their loss because of the operation of selective forces or by chance . If one is willing to make the assumption that the protein variants under study are essentially neutral with reference to their ...
Seite 86
... protein , the nature of the association and the packing problem Chromatin contains an approximately equal amount by weight of DNA and protein , the major protein component being basic proteins or histones . Accepting that the DNA is ...
... protein , the nature of the association and the packing problem Chromatin contains an approximately equal amount by weight of DNA and protein , the major protein component being basic proteins or histones . Accepting that the DNA is ...
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