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 30
Seite 155
... MALFORMATIONS IN MAN * JOHN M. OPITZ Wisconsin Clinical Genetics Center , Department of Medical Genetics , University of Wisconsin Center for Health Sciences and Medical School , Madison , Wis . , U.S.A. Nomina si nescis , perit et ...
... MALFORMATIONS IN MAN * JOHN M. OPITZ Wisconsin Clinical Genetics Center , Department of Medical Genetics , University of Wisconsin Center for Health Sciences and Medical School , Madison , Wis . , U.S.A. Nomina si nescis , perit et ...
Seite 171
... malformations A number of techniques have been explored for their possible value in diagnosing CNS malformations ( anencephaly and spina bifida ) in utero . These have included sonography , foetoscopy , the study of amniotic fluid ...
... malformations A number of techniques have been explored for their possible value in diagnosing CNS malformations ( anencephaly and spina bifida ) in utero . These have included sonography , foetoscopy , the study of amniotic fluid ...
Seite 172
... malformations are born to mothers with no previous family history . If a significant proportion of these malformations is to be prevented , then the entire population needs to be screened but amniocentesis could not be used for this ...
... malformations are born to mothers with no previous family history . If a significant proportion of these malformations is to be prevented , then the entire population needs to be screened but amniocentesis could not be used for this ...
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