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 22
... approach than in the study of sentinel phenotypes . The approach will permit much more accurate interspecific comparisons , since a comparable enzyme in a series of species must usually be associated with homologous genes . This fact is ...
... approach than in the study of sentinel phenotypes . The approach will permit much more accurate interspecific comparisons , since a comparable enzyme in a series of species must usually be associated with homologous genes . This fact is ...
Seite 23
... approaches . Examples of the application of the relative approach Two examples of the relative approach will suffice . In a series of papers now in press , my Japanese and American colleagues and I have presented data on the frequency ...
... approaches . Examples of the application of the relative approach Two examples of the relative approach will suffice . In a series of papers now in press , my Japanese and American colleagues and I have presented data on the frequency ...
Seite 30
... approach , starting now , although in theory , with 3 - generation studies , we could reach back 1 generation . The recent discussions of possible procedures for monitoring germinal mutation rates have for the most part centered on the ...
... approach , starting now , although in theory , with 3 - generation studies , we could reach back 1 generation . The recent discussions of possible procedures for monitoring germinal mutation rates have for the most part centered on the ...
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