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

Year Number of Results
1921 1
1938 1
1950 1
1961 1
1981 2
1986 2
1987 1
1989 1
1994 2
1995 1
1996 4
1997 1
1998 3
1999 3
2000 4
2001 2
2003 2
2004 3
2006 1
2007 3
2008 5
2009 6
2010 3
2011 3
2012 3
2013 11
2014 6
2015 4
2016 3
2017 2
2018 3
2019 5
2020 5
2021 6
2022 1
2024 0

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Similar articles for PMID: 19369601

98 results

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Page 1
Prenatal diagnosis of MPPH syndrome.
De Keersmaecker B, Van Esch H, Van Schoubroeck D, Claus F, Moerman P, De Catte L. De Keersmaecker B, et al. Prenat Diagn. 2013 Mar;33(3):292-5. doi: 10.1002/pd.4039. Epub 2013 Jan 24. Prenat Diagn. 2013. PMID: 23348821
Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis.
Mirzaa GM, Conway RL, Gripp KW, Lerman-Sagie T, Siegel DH, deVries LS, Lev D, Kramer N, Hopkins E, Graham JM Jr, Dobyns WB. Mirzaa GM, et al. Am J Med Genet A. 2012 Feb;158A(2):269-91. doi: 10.1002/ajmg.a.34402. Epub 2012 Jan 6. Am J Med Genet A. 2012. PMID: 22228622
MPPH syndrome: two new cases.
Osterling WL, Boyer RS, Hedlund GL, Bale JF Jr. Osterling WL, et al. Pediatr Neurol. 2011 May;44(5):370-3. doi: 10.1016/j.pediatrneurol.2010.12.009. Pediatr Neurol. 2011. PMID: 21481746
Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus.
Verkerk AJ, Schot R, van Waterschoot L, Douben H, Poddighe PJ, Lequin MH, de Vries LS, Terhal P, Hahnemann JM, de Coo IF, de Wit MC, Wafelman LS, Garavelli L, Dobyns WB, Van der Spek PJ, de Klein A, Mancini GM. Verkerk AJ, et al. Am J Med Genet A. 2010 Jun;152A(6):1488-97. doi: 10.1002/ajmg.a.33408. Am J Med Genet A. 2010. PMID: 20503325 Free PMC article.
98 results