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

Year Number of Results
1978 1
1983 1
1985 1
1993 1
1995 1
1996 1
1999 3
2000 2
2001 2
2002 3
2003 3
2004 5
2005 8
2006 13
2007 10
2008 10
2009 8
2010 11
2011 11
2012 7
2013 6
2014 2
2015 2
2016 5
2017 3
2018 4
2019 6
2020 2
2021 3
2022 3
2024 0

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Similar articles for PMID: 17632775

120 results

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Page 1
Filamin A mutation is one cause of FG syndrome.
Unger S, Mainberger A, Spitz C, Bähr A, Zeschnigk C, Zabel B, Superti-Furga A, Morris-Rosendahl DJ. Unger S, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1876-9. doi: 10.1002/ajmg.a.31751. Am J Med Genet A. 2007. PMID: 17632775
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
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome.
Sheen VL, Jansen A, Chen MH, Parrini E, Morgan T, Ravenscroft R, Ganesh V, Underwood T, Wiley J, Leventer R, Vaid RR, Ruiz DE, Hutchins GM, Menasha J, Willner J, Geng Y, Gripp KW, Nicholson L, Berry-Kravis E, Bodell A, Apse K, Hill RS, Dubeau F, Andermann F, Barkovich J, Andermann E, Shugart YY, Thomas P, Viri M, Veggiotti P, Robertson S, Guerrini R, Walsh CA. Sheen VL, et al. Neurology. 2005 Jan 25;64(2):254-62. doi: 10.1212/01.WNL.0000149512.79621.DF. Neurology. 2005. PMID: 15668422
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations.
Parrini E, Ramazzotti A, Dobyns WB, Mei D, Moro F, Veggiotti P, Marini C, Brilstra EH, Dalla Bernardina B, Goodwin L, Bodell A, Jones MC, Nangeroni M, Palmeri S, Said E, Sander JW, Striano P, Takahashi Y, Van Maldergem L, Leonardi G, Wright M, Walsh CA, Guerrini R. Parrini E, et al. Brain. 2006 Jul;129(Pt 7):1892-906. doi: 10.1093/brain/awl125. Epub 2006 May 9. Brain. 2006. PMID: 16684786
120 results