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

Year Number of Results
1982 2
1983 1
1984 1
1993 1
1995 1
1997 1
1998 1
1999 1
2000 1
2001 1
2002 4
2003 3
2004 2
2005 4
2006 5
2007 19
2008 13
2009 7
2010 1
2011 3
2012 1
2013 3
2015 1
2016 4
2017 2
2021 3
2022 2
2023 1
2024 0

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Similar articles for PMID: 17334363

82 results

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Page 1
Genitourinary anomalies of pediatric FG syndrome.
Smith JF, Wayment RO, Cartwright PC, Snow BW, Opitz JM. Smith JF, et al. J Urol. 2007 Aug;178(2):656-9. doi: 10.1016/j.juro.2007.04.007. Epub 2007 Jun 15. J Urol. 2007. PMID: 17574621
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene.
Schwartz CE, Tarpey PS, Lubs HA, Verloes A, May MM, Risheg H, Friez MJ, Futreal PA, Edkins S, Teague J, Briault S, Skinner C, Bauer-Carlin A, Simensen RJ, Joseph SM, Jones JR, Gecz J, Stratton MR, Raymond FL, Stevenson RE. Schwartz CE, et al. J Med Genet. 2007 Jul;44(7):472-7. doi: 10.1136/jmg.2006.048637. Epub 2007 Mar 16. J Med Genet. 2007. PMID: 17369503 Free PMC article.
MED12 related disorders.
Graham JM Jr, Schwartz CE. Graham JM Jr, et al. Am J Med Genet A. 2013 Nov;161A(11):2734-40. doi: 10.1002/ajmg.a.36183. Epub 2013 Oct 10. Am J Med Genet A. 2013. PMID: 24123922 Free PMC article. Review.
A gene for FG syndrome maps in the Xq12-q21.31 region.
Briault S, Hill R, Shrimpton A, Zhu D, Till M, Ronce N, Margaritte-Jeannin P, Baraitser M, Middleton-Price H, Malcolm S, Thompson E, Hoo J, Wilson G, Romano C, Guichet A, Pembrey M, Fontes M, Poustka A, Moraine C. Briault S, et al. Am J Med Genet. 1997 Nov 28;73(1):87-90. Am J Med Genet. 1997. PMID: 9375929
82 results