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

Year Number of Results
1958 2
1964 1
1965 1
2005 1
2008 1
2012 3
2013 3
2014 2
2015 2
2016 3
2017 2
2018 1
2022 2
2023 2
2024 0

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Page 1
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Rivière JB, Mirzaa GM, O'Roak BJ, Beddaoui M, Alcantara D, Conway RL, St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GM, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Zirn B, Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, Shendure J, Graham JM Jr, Boycott KM, Dobyns WB. Rivière JB, et al. Among authors: sullivan ct. Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331. Nat Genet. 2012. PMID: 22729224 Free PMC article.
X Chromosome-Inactivation Patterns in 31 Individuals with PHACE Syndrome.
Sullivan CT, Christian SL, Shieh JT, Metry D, Blei F, Krol A, Drolet BA, Frieden IJ, Dobyns WB, Siegel DH. Sullivan CT, et al. Mol Syndromol. 2013 Mar;4(3):114-8. doi: 10.1159/000343489. Epub 2012 Nov 16. Mol Syndromol. 2013. PMID: 23653582 Free PMC article.
22 results