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

Year Number of Results
1913 1
1927 1
1960 1
1971 1
1981 1
1983 1
1986 1
1989 1
1990 1
1994 1
1996 1
1997 1
1999 1
2000 2
2001 1
2002 1
2003 2
2004 2
2005 3
2006 2
2007 1
2008 1
2009 1
2010 3
2011 3
2012 3
2013 6
2014 8
2015 10
2016 5
2017 4
2018 2
2019 2
2020 1
2021 1
2022 1
2024 0

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Similar articles for PMID: 27640920

70 results

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Page 1
Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis.
Schrauwen I, Valgaeren H, Tomas-Roca L, Sommen M, Altunoglu U, Wesdorp M, Beyens M, Fransen E, Nasir A, Vandeweyer G, Schepers A, Rahmoun M, van Beusekom E, Huentelman MJ, Offeciers E, Dhooghe I, Huber A, Van de Heyning P, Zanetti D, De Leenheer EMR, Gilissen C, Hoischen A, Cremers CW, Verbist B, de Brouwer APM, Padberg GW, Pennings R, Kayserili H, Kremer H, Van Camp G, van Bokhoven H. Schrauwen I, et al. Genet Med. 2019 May;21(5):1199-1208. doi: 10.1038/s41436-018-0300-5. Epub 2018 Oct 5. Genet Med. 2019. PMID: 30287925 Free article.
The congenital cranial dysinnervation disorders.
Gutowski NJ, Chilton JK. Gutowski NJ, et al. Arch Dis Child. 2015 Jul;100(7):678-81. doi: 10.1136/archdischild-2014-307035. Epub 2015 Jan 29. Arch Dis Child. 2015. PMID: 25633065 Review.
70 results