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Page 1
Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe.
Barisic I, Boban L, Akhmedzhanova D, Bergman JEH, Cavero-Carbonell C, Grinfelde I, Materna-Kiryluk A, Latos-Bieleńska A, Randrianaivo H, Zymak-Zakutnya N, Sansovic I, Lanzoni M, Morris JK. Barisic I, et al. Among authors: morris jk. Eur J Med Genet. 2018 Sep;61(9):499-507. doi: 10.1016/j.ejmg.2018.05.014. Epub 2018 May 31. Eur J Med Genet. 2018. PMID: 29753922
Is the prevalence of Klinefelter syndrome increasing?
Morris JK, Alberman E, Scott C, Jacobs P. Morris JK, et al. Eur J Hum Genet. 2008 Feb;16(2):163-70. doi: 10.1038/sj.ejhg.5201956. Epub 2007 Nov 14. Eur J Hum Genet. 2008. PMID: 18000523
Valproic acid monotherapy in pregnancy and major congenital malformations.
Jentink J, Loane MA, Dolk H, Barisic I, Garne E, Morris JK, de Jong-van den Berg LT; EUROCAT Antiepileptic Study Working Group. Jentink J, et al. Among authors: morris jk. N Engl J Med. 2010 Jun 10;362(23):2185-93. doi: 10.1056/NEJMoa0907328. N Engl J Med. 2010. PMID: 20558369 Free article. Review.
Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening.
Loane M, Morris JK, Addor MC, Arriola L, Budd J, Doray B, Garne E, Gatt M, Haeusler M, Khoshnood B, Klungsøyr Melve K, Latos-Bielenska A, McDonnell B, Mullaney C, O'Mahony M, Queisser-Wahrendorf A, Rankin J, Rissmann A, Rounding C, Salvador J, Tucker D, Wellesley D, Yevtushok L, Dolk H. Loane M, et al. Among authors: morris jk. Eur J Hum Genet. 2013 Jan;21(1):27-33. doi: 10.1038/ejhg.2012.94. Epub 2012 Jun 20. Eur J Hum Genet. 2013. PMID: 22713804 Free PMC article.
Birth prevalence and survival of exomphalos in england and wales: 2005 to 2011.
Springett A, Draper ES, Rankin J, Rounding C, Tucker D, Stoianova S, Wellesley D, Morris JK. Springett A, et al. Among authors: morris jk. Birth Defects Res A Clin Mol Teratol. 2014 Sep;100(9):721-5. doi: 10.1002/bdra.23301. Epub 2014 Sep 1. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25178262
Major congenital anomalies in babies born with Down syndrome: a EUROCAT population-based registry study.
Morris JK, Garne E, Wellesley D, Addor MC, Arriola L, Barisic I, Beres J, Bianchi F, Budd J, Dias CM, Gatt M, Klungsoyr K, Khoshnood B, Latos-Bielenska A, Mullaney C, Nelen V, Neville AJ, O'Mahony M, Queisser-Luft A, Randrianaivo H, Rankin J, Rissmann A, Rounding C, Sipek A, Stoianova S, Tucker D, de Walle H, Yevtushok L, Loane M, Dolk H. Morris JK, et al. Am J Med Genet A. 2014 Dec;164A(12):2979-86. doi: 10.1002/ajmg.a.36780. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25257471
Congenital anomalies associated with trisomy 18 or trisomy 13: A registry-based study in 16 European countries, 2000-2011.
Springett A, Wellesley D, Greenlees R, Loane M, Addor MC, Arriola L, Bergman J, Cavero-Carbonell C, Csaky-Szunyogh M, Draper ES, Garne E, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Lynch C, Dias CM, McDonnell R, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Stoianova S, Tuckerz D, Zymak-Zakutnia N, Morris JK. Springett A, et al. Among authors: morris jk. Am J Med Genet A. 2015 Dec;167A(12):3062-9. doi: 10.1002/ajmg.a.37355. Epub 2015 Sep 8. Am J Med Genet A. 2015. PMID: 26347425
343 results