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Page 1
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.
Wellesley D, Dolk H, Boyd PA, Greenlees R, Haeusler M, Nelen V, Garne E, Khoshnood B, Doray B, Rissmann A, Mullaney C, Calzolari E, Bakker M, Salvador J, Addor MC, Draper E, Rankin J, Tucker D. Wellesley D, et al. Eur J Hum Genet. 2012 May;20(5):521-6. doi: 10.1038/ejhg.2011.246. Epub 2012 Jan 11. Eur J Hum Genet. 2012. PMID: 22234154 Free PMC article.
Fraser syndrome: epidemiological study in a European population.
Barisic I, Odak L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Arriola L, Bergman J, Bianca S, Boyd PA, Draper ES, Gatt M, Haeusler M, Khoshnood B, Latos-Bielenska A, McDonnell B, Pierini A, Rankin J, Rissmann A, Queisser-Luft A, Verellen-Dumoulin C, Stone D, Tenconi R. Barisic I, et al. Am J Med Genet A. 2013 May;161A(5):1012-8. doi: 10.1002/ajmg.a.35839. Epub 2013 Mar 26. Am J Med Genet A. 2013. PMID: 23532946
Prevalence of congenital anomalies in five British regions, 1991-99.
Rankin J, Pattenden S, Abramsky L, Boyd P, Jordan H, Stone D, Vrijheid M, Wellesley D, Dolk H. Rankin J, et al. Among authors: boyd p. Arch Dis Child Fetal Neonatal Ed. 2005 Sep;90(5):F374-9. doi: 10.1136/adc.2003.047902. Arch Dis Child Fetal Neonatal Ed. 2005. PMID: 16113153 Free PMC article.
Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007.
Boyle B, McConkey R, Garne E, Loane M, Addor MC, Bakker MK, Boyd PA, Gatt M, Greenlees R, Haeusler M, Klungsøyr K, Latos-Bielenska A, Lelong N, McDonnell R, Métneki J, Mullaney C, Nelen V, O'Mahony M, Pierini A, Rankin J, Rissmann A, Tucker D, Wellesley D, Dolk H. Boyle B, et al. Among authors: boyd pa. BJOG. 2013 May;120(6):707-16. doi: 10.1111/1471-0528.12146. Epub 2013 Feb 6. BJOG. 2013. PMID: 23384325
529 results