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Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.
Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, Sherman SL. Crawford DC, et al. Among authors: brown wt. Am J Hum Genet. 2000 Feb;66(2):480-93. doi: 10.1086/302762. Am J Hum Genet. 2000. PMID: 10677308 Free PMC article.
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.
Familial transmission of the FMR1 CGG repeat.
Nolin SL, Lewis FA 3rd, Ye LL, Houck GE Jr, Glicksman AE, Limprasert P, Li SY, Zhong N, Ashley AE, Feingold E, Sherman SL, Brown WT. Nolin SL, et al. Among authors: brown wt. Am J Hum Genet. 1996 Dec;59(6):1252-61. Am J Hum Genet. 1996. PMID: 8940270 Free PMC article.
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
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
398 results