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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1971 1
1979 1
1981 1
1983 1
1984 2
1985 2
1986 1
1988 2
1989 2
1991 1
1992 3
1993 3
1994 4
1995 2
1996 5
1997 3
1998 1
1999 4
2000 5
2001 4
2002 1
2003 10
2004 3
2005 2
2006 3
2007 2
2008 1
2009 4
2010 9
2011 13
2012 7
2013 7
2014 5
2015 3
2016 4
2017 4
2018 5
2019 2
2020 2
2021 1
2022 1
2023 1
2024 0

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126 results

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Page 1
HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients.
Moortgat S, Berland S, Aukrust I, Maystadt I, Baker L, Benoit V, Caro-Llopis A, Cooper NS, Debray FG, Faivre L, Gardeitchik T, Haukanes BI, Houge G, Kivuva E, Martinez F, Mehta SG, Nassogne MC, Powell-Hamilton N, Pfundt R, Rosello M, Prescott T, Vasudevan P, van Loon B, Verellen-Dumoulin C, Verloes A, Lippe CV, Wakeling E, Wilkie AOM, Wilson L, Yuen A, Study D, Low KJ, Newbury-Ecob RA. Moortgat S, et al. Among authors: verellen dumoulin c. Eur J Hum Genet. 2018 Jan;26(1):64-74. doi: 10.1038/s41431-017-0038-6. Epub 2017 Nov 27. Eur J Hum Genet. 2018. PMID: 29180823 Free PMC article.
Paper 6: EUROCAT member registries: organization and activities.
Greenlees R, Neville A, Addor MC, Amar E, Arriola L, Bakker M, Barisic I, Boyd PA, Calzolari E, Doray B, Draper E, Vollset SE, Garne E, Gatt M, Haeusler M, Kallen K, Khoshnood B, Latos-Bielenska A, Martinez-Frias ML, Materna-Kiryluk A, Dias CM, McDonnell B, Mullaney C, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Randrianaivo-Ranjatoélina H, Rankin J, Rissmann A, Ritvanen A, Salvador J, Sipek A, Tucker D, Verellen-Dumoulin C, Wellesley D, Wertelecki W. Greenlees R, et al. Among authors: verellen dumoulin c. Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1:S51-S100. doi: 10.1002/bdra.20775. Epub 2011 Mar 4. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21381185 Free article. Review.
Dicentric (1;15) in myeloid disorders.
Michaux L, Dierlamm J, Mecucci C, Meeus P, Ameye G, Libouton JM, Verhoef G, Ferrant A, Louwagie A, Verellen-Dumoulin C, Van Den Berghe H. Michaux L, et al. Among authors: verellen dumoulin c. Cancer Genet Cytogenet. 1996 May;88(1):86-9. doi: 10.1016/0165-4608(95)00218-9. Cancer Genet Cytogenet. 1996. PMID: 8630988 Review.
Congenital clubfoot in Europe: A population-based study.
Wang H, Barisic I, Loane M, Addor MC, Bailey LM, Gatt M, Klungsoyr K, Mokoroa O, Nelen V, Neville AJ, O'Mahony M, Pierini A, Rissmann A, Verellen-Dumoulin C, de Walle HEK, Wiesel A, Wisniewska K, de Jong-van den Berg LTW, Dolk H, Khoshnood B, Garne E. Wang H, et al. Among authors: verellen dumoulin c. Am J Med Genet A. 2019 Apr;179(4):595-601. doi: 10.1002/ajmg.a.61067. Epub 2019 Feb 10. Am J Med Genet A. 2019. PMID: 30740879
Paper 2: EUROCAT public health indicators for congenital anomalies in Europe.
Khoshnood B, Greenlees R, Loane M, Dolk H; EUROCAT Project Management Committee; EUROCAT Working Group. Khoshnood B, et al. Birth Defects Res A Clin Mol Teratol. 2011 Mar;91 Suppl 1(Suppl 1):S16-22. doi: 10.1002/bdra.20776. Epub 2011 Mar 4. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21381186 Free PMC article. Review.
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. 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.
Atypical findings in three patients with Pai syndrome and literature review.
Lederer D, Wilson B, Lefesvre P, Poorten VV, Kirkham N, Mitra D, Verellen-Dumoulin C, Devriendt K. Lederer D, et al. Among authors: verellen dumoulin c. Am J Med Genet A. 2012 Nov;158A(11):2899-904. doi: 10.1002/ajmg.a.35592. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987662 Review.
126 results