Brown WT - Search Results

1

Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.

Nolin SL, Glicksman A, Ersalesi N, Dobkin C, Brown WT, Cao R, Blatt E, Sah S, Latham GJ, Hadd AG. Nolin SL, et al. Among authors: brown wt. Genet Med. 2015 May;17(5):358-64. doi: 10.1038/gim.2014.106. Epub 2014 Sep 11. Genet Med. 2015. PMID: 25210937 Free article.

2

Fragile X prenatal analyses show full mutation females at high risk for mosaic Turner syndrome: fragile X leads to chromosome loss.

Dobkin C, Radu G, Ding XH, Brown WT, Nolin SL. Dobkin C, et al. Among authors: brown wt. Am J Med Genet A. 2009 Oct;149A(10):2152-7. doi: 10.1002/ajmg.a.33011. Am J Med Genet A. 2009. PMID: 19764037

3

Fragile X analysis of 1112 prenatal samples from 1991 to 2010.

Nolin SL, Glicksman A, Ding X, Ersalesi N, Brown WT, Sherman SL, Dobkin C. Nolin SL, et al. Among authors: brown wt. Prenat Diagn. 2011 Oct;31(10):925-31. doi: 10.1002/pd.2815. Epub 2011 Jun 30. Prenat Diagn. 2011. PMID: 21717484

4

Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.

Nolin SL, Sah S, Glicksman A, Sherman SL, Allen E, Berry-Kravis E, Tassone F, Yrigollen C, Cronister A, Jodah M, Ersalesi N, Dobkin C, Brown WT, Shroff R, Latham GJ, Hadd AG. Nolin SL, et al. Among authors: brown wt. Am J Med Genet A. 2013 Apr;161A(4):771-8. doi: 10.1002/ajmg.a.35833. Epub 2013 Feb 26. Am J Med Genet A. 2013. PMID: 23444167 Free PMC article.

5

Fragile X protein in newborn dried blood spots.

Adayev T, LaFauci G, Dobkin C, Caggana M, Wiley V, Field M, Wotton T, Kascsak R, Nolin SL, Glicksman A, Hosmer N, Brown WT. Adayev T, et al. Among authors: brown wt. BMC Med Genet. 2014 Oct 28;15:119. doi: 10.1186/s12881-014-0119-0. BMC Med Genet. 2014. PMID: 25348928 Free PMC article.

6

Molecular analysis of fragile X syndrome.

Nolin SL, Dobkin C, Brown WT. Nolin SL, et al. Among authors: brown wt. Curr Protoc Hum Genet. 2003 Nov;Chapter 9:Unit9.5. doi: 10.1002/0471142905.hg0905s38. Curr Protoc Hum Genet. 2003. PMID: 18428348

7

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.

Nolin SL, Brown WT, Glicksman A, Houck GE Jr, Gargano AD, Sullivan A, Biancalana V, Bröndum-Nielsen K, Hjalgrim H, Holinski-Feder E, Kooy F, Longshore J, Macpherson J, Mandel JL, Matthijs G, Rousseau F, Steinbach P, Väisänen ML, von Koskull H, Sherman SL. Nolin SL, et al. Among authors: brown wt. Am J Hum Genet. 2003 Feb;72(2):454-64. doi: 10.1086/367713. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529854 Free PMC article.

8

Fragile X full mutation alleles composed of few alleles: implications for CGG repeat expansion.

Nolin SL, Ding XH, Houck GE, Brown WT, Dobkin C. Nolin SL, et al. Among authors: brown wt. Am J Med Genet A. 2008 Jan 1;146A(1):60-5. doi: 10.1002/ajmg.a.32087. Am J Med Genet A. 2008. PMID: 18074381

9

Fragile X screening program in New York State.

Nolin SL, Snider DA, Jenkins EC, Brown WT, Krawczun M, Stetka D, Houck G Jr, Dobkin CS, Strong G, Smith-Dobransky G, et al. Nolin SL, et al. Among authors: brown wt. Am J Med Genet. 1991 Feb-Mar;38(2-3):251-5. doi: 10.1002/ajmg.1320380218. Am J Med Genet. 1991. PMID: 2018068

10

Pulsed-field gradient-gel studies around the fragile site.

Dobkin CS, Brown WT. Dobkin CS, et al. Among authors: brown wt. Am J Med Genet. 1988 May-Jun;30(1-2):593-600. doi: 10.1002/ajmg.1320300160. Am J Med Genet. 1988. PMID: 2902798

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