Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
Ergebnisse 1-3 von 59
Seite 174
... diagnosis has been an extremely important development in medical genetics , but it is not without problems . Quite apart from the technical problems and the ethical issues raised by selective abortion , there are the obstetric and ...
... diagnosis has been an extremely important development in medical genetics , but it is not without problems . Quite apart from the technical problems and the ethical issues raised by selective abortion , there are the obstetric and ...
Seite 195
... diagnosis . To inspire confidence in prenatal monitoring the quality of the analyses should be optimal . Since the incidence of most ... diagnosis of metabolic disorders . Unfortunately , the results Microtechniques in prenatal diagnosis 195.
... diagnosis . To inspire confidence in prenatal monitoring the quality of the analyses should be optimal . Since the incidence of most ... diagnosis of metabolic disorders . Unfortunately , the results Microtechniques in prenatal diagnosis 195.
Seite 207
... 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 detection of genetic disorders ...
... 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 detection of genetic disorders ...
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 | |
30 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
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