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 68
Seite 46
... detected and 15 of these were seen on non - banded preparations , while only 1 was missed on orcein - stained slides and subsequently detected using G - banding . Thus , in this material , over half of which comes from populations of ...
... detected and 15 of these were seen on non - banded preparations , while only 1 was missed on orcein - stained slides and subsequently detected using G - banding . Thus , in this material , over half of which comes from populations of ...
Seite 188
... detected at amniocentesis and a male baby was born ; and in 1 case a male was diagnosed and a female was born . The 2 false negatives both resulted in a missed diagnosis of Down's syndrome : in 1 case , a normal female was detected at ...
... detected at amniocentesis and a male baby was born ; and in 1 case a male was diagnosed and a female was born . The 2 false negatives both resulted in a missed diagnosis of Down's syndrome : in 1 case , a normal female was detected at ...
Seite 192
... detected while a female with Down's syndrome was born . The use of chromosome banding and identification of appropriate marker chromosomes in the parents followed by banding of the ' fetal ' chromosomes and a search for paternally ...
... detected while a female with Down's syndrome was born . The use of chromosome banding and identification of appropriate marker chromosomes in the parents followed by banding of the ' fetal ' chromosomes and a search for paternally ...
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