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 54
... chemical mutagens and / or carcinogens . There could be another long list with compounds on which conflicting or false positive results have been published . Time does not permit me to cover this aspect of the problem . As regards the ...
... chemical mutagens and / or carcinogens . There could be another long list with compounds on which conflicting or false positive results have been published . Time does not permit me to cover this aspect of the problem . As regards the ...
Seite 367
... chemical mutagens and chemical carcinogens . This same process of activation may occur unequally among individuals of animal and human populations , with the result that some individuals may be much more sensitive than others to chemical ...
... chemical mutagens and chemical carcinogens . This same process of activation may occur unequally among individuals of animal and human populations , with the result that some individuals may be much more sensitive than others to chemical ...
Seite 406
... Chemical carcinogenesis Less is known about genetic predisposition to chemical carcinogens . Xeroderma pigmentosum and ataxia telangiectasia may both prove to be examples of such a predisposition . In xeroderma pigmentosum the defect in ...
... Chemical carcinogenesis Less is known about genetic predisposition to chemical carcinogens . Xeroderma pigmentosum and ataxia telangiectasia may both prove to be examples of such a predisposition . In xeroderma pigmentosum the defect in ...
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