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

Year Number of Results
1993 1
2002 4
2003 6
2004 6
2005 4
2006 1
2007 2
2008 5
2009 6
2010 7
2011 9
2012 13
2013 10
2014 11
2015 7
2016 5
2017 7
2018 2
2020 1
2021 1
2022 2
2023 3
2024 0

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102 results

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Page 1
Hutchinson-Gilford Progeria Syndrome.
Gordon LB, Brown WT, Collins FS. Gordon LB, et al. Among authors: brown wt. 2003 Dec 12 [updated 2023 Oct 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Dec 12 [updated 2023 Oct 19]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301300 Free Books & Documents. Review.
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Among authors: brown wt. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC article.
Fragile X targeted pharmacotherapy: lessons learned and future directions.
Erickson CA, Davenport MH, Schaefer TL, Wink LK, Pedapati EV, Sweeney JA, Fitzpatrick SE, Brown WT, Budimirovic D, Hagerman RJ, Hessl D, Kaufmann WE, Berry-Kravis E. Erickson CA, et al. Among authors: brown wt. J Neurodev Disord. 2017 Jun 12;9:7. doi: 10.1186/s11689-017-9186-9. eCollection 2017. J Neurodev Disord. 2017. PMID: 28616096 Free PMC article. Review.
Genes associated with autism spectrum disorder.
Li X, Zou H, Brown WT. Li X, et al. Among authors: brown wt. Brain Res Bull. 2012 Sep 1;88(6):543-52. doi: 10.1016/j.brainresbull.2012.05.017. Epub 2012 Jun 9. Brain Res Bull. 2012. PMID: 22688012 Review.
Prospects for gene therapy in the fragile X syndrome.
Rattazzi MC, LaFauci G, Brown WT. Rattazzi MC, et al. Among authors: brown wt. Ment Retard Dev Disabil Res Rev. 2004;10(1):75-81. doi: 10.1002/mrdd.20012. Ment Retard Dev Disabil Res Rev. 2004. PMID: 14994292 Review.
102 results