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219 results

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Page 1
Mosaicism in fragile X affected males.
Nolin SL, Glicksman A, Houck GE Jr, Brown WT, Dobkin CS. Nolin SL, et al. Among authors: glicksman a. Am J Med Genet. 1994 Jul 15;51(4):509-12. doi: 10.1002/ajmg.1320510444. Am J Med Genet. 1994. PMID: 7943031
Prenatal diagnosis and carrier screening for fragile X by PCR.
Brown WT, Nolin S, Houck G Jr, Ding X, Glicksman A, Li SY, Stark-Houck S, Brophy P, Duncan C, Dobkin C, Jenkins E. Brown WT, et al. Among authors: glicksman a. Am J Med Genet. 1996 Jul 12;64(1):191-5. doi: 10.1002/(SICI)1096-8628(19960712)64:1<191::AID-AJMG34>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826474
Reverse mutations in the fragile X syndrome.
Brown WT, Houck GE Jr, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, Jenkins EC. Brown WT, et al. Among authors: glicksman a. Am J Med Genet. 1996 Aug 9;64(2):287-92. doi: 10.1002/(SICI)1096-8628(19960809)64:2<287::AID-AJMG11>3.0.CO;2-B. Am J Med Genet. 1996. PMID: 8844067
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: glicksman ae. Am J Hum Genet. 1996 Dec;59(6):1252-61. Am J Hum Genet. 1996. PMID: 8940270 Free PMC article.
Examination of factors associated with instability of the FMR1 CGG repeat.
Ashley-Koch AE, Robinson H, Glicksman AE, Nolin SL, Schwartz CE, Brown WT, Turner G, Sherman SL. Ashley-Koch AE, et al. Among authors: glicksman ae. Am J Hum Genet. 1998 Sep;63(3):776-85. doi: 10.1086/302018. Am J Hum Genet. 1998. PMID: 9718348 Free PMC article.
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data.
Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJ, Yang KT, Lee C, Hudson R, Gorwill H, Nolin SL, Glicksman A, Jenkins EC, Brown WT, Howard-Peebles PN, Becchi C, Cummings E, Fallon L, Seitz S, Black SH, Vianna-Morgante AM, Costa SS, Otto PA, Mingroni-Netto RC, Murray A, Webb J, Vieri F, et al. Allingham-Hawkins DJ, et al. Among authors: glicksman a. Am J Med Genet. 1999 Apr 2;83(4):322-5. Am J Med Genet. 1999. PMID: 10208170 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: glicksman a. 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.
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: glicksman a. Prenat Diagn. 2011 Oct;31(10):925-31. doi: 10.1002/pd.2815. Epub 2011 Jun 30. Prenat Diagn. 2011. PMID: 21717484
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: glicksman a. 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.
219 results