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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. 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.
Molecular analysis of fragile X syndrome.
Nolin SL, Dobkin C, Brown WT. Nolin SL, et al. Curr Protoc Hum Genet. 2003 Nov;Chapter 9:Unit9.5. doi: 10.1002/0471142905.hg0905s38. Curr Protoc Hum Genet. 2003. PMID: 18428348
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. 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.
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: nolin sl. BMC Med Genet. 2014 Oct 28;15:119. doi: 10.1186/s12881-014-0119-0. BMC Med Genet. 2014. PMID: 25348928 Free PMC article.
46 results