Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe
- 11 January 2012
- journal article
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 20 (5), 521-526
- https://doi.org/10.1038/ejhg.2011.246
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancyEuropean Journal of Human Genetics, 2010
- The European Perinatal Health Report: comparing the health and care of pregnant women and newborn babies in EuropeJournal of Epidemiology and Community Health, 2009
- Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocentesesEuropean Journal of Human Genetics, 2009
- Survey of prenatal screening policies in Europe for structural malformations and chromosome anomalies, and their impact on detection and termination rates for neural tube defects and Down’s syndromeBJOG: An International Journal of Obstetrics and Gynaecology, 2008
- Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort studyHuman Genetics, 2008
- Patterns of chromosomal deletions identified by a birth defects registry, Hawaii, 1986?2003Congenital Anomalies, 2007
- Epidemiology of triploidy in a population‐based birth defects registry, Hawaii, 1986–1999American Journal of Medical Genetics Part A, 2003
- Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in rhus, DenmarkHuman Genetics, 1991
- Frequency of births with potentially avoidable serious chromosomal anomalies in EEC countries, 1979-1982.Journal of Epidemiology and Community Health, 1988
- A total population study of diagnosed chromosome abnormalities in Queens land, AustraliaClinical Genetics, 1982