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 19
... recent advances in our understanding of the nature and frequency of mutation have not been proportional to recent advances in other fields of genetic endeavor . In higher organisms the principal indicators of a mutational event which it ...
... recent advances in our understanding of the nature and frequency of mutation have not been proportional to recent advances in other fields of genetic endeavor . In higher organisms the principal indicators of a mutational event which it ...
Seite 207
... RECENT ADVANCES IN PRENATAL GENETIC DIAGNOSIS HENRY L. NADLER Division of Genetics , The Children's Memorial Hospital and Department of Pediatrics , Northwestern University Medical School , Chicago , Ill . , U.S.A. The intrauterine ...
... RECENT ADVANCES IN PRENATAL GENETIC DIAGNOSIS HENRY L. NADLER Division of Genetics , The Children's Memorial Hospital and Department of Pediatrics , Northwestern University Medical School , Chicago , Ill . , U.S.A. The intrauterine ...
Seite 341
... recent review ( Fraumeni , 1975a ) are summarized here . Tobacco , in the form of cigarette smoking , is recognized as the principal cause of cancers of the lung , larynx , and oral cavity . Smoking also accounts for a portion of ...
... recent review ( Fraumeni , 1975a ) are summarized here . Tobacco , in the form of cigarette smoking , is recognized as the principal cause of cancers of the lung , larynx , and oral cavity . Smoking also accounts for a portion of ...
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