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 16
... changes in a population , nor can it be used to say anything about the plasticity of the trait under environmental manipulation . The degree to which a genetic disease may be curable , or the degree to which normal human variation can ...
... changes in a population , nor can it be used to say anything about the plasticity of the trait under environmental manipulation . The degree to which a genetic disease may be curable , or the degree to which normal human variation can ...
Seite 33
... changes in the chemical composition and functional capacity of individual cells . This being so , we can inquire as to what part the genome plays in determining these changes . In effect , this is to ask what changes single mutations ...
... changes in the chemical composition and functional capacity of individual cells . This being so , we can inquire as to what part the genome plays in determining these changes . In effect , this is to ask what changes single mutations ...
Seite 284
... changes underlies cell differentiation , and since the molecular bases of these changes are unknown , they can be defined only in terms of their consequences for the cell's potentiality and fate . One of the earliest of these changes is ...
... changes underlies cell differentiation , and since the molecular bases of these changes are unknown , they can be defined only in terms of their consequences for the cell's potentiality and fate . One of the earliest of these changes 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