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Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers.
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.
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: ersalesi n.
Prenat Diagn. 2011 Oct;31(10):925-31. doi: 10.1002/pd.2815. Epub 2011 Jun 30.
Prenat Diagn. 2011.
PMID: 21717484
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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: ersalesi n.
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.
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Cis-acting DNA sequence at a replication origin promotes repeat expansion to fragile X full mutation.
Gerhardt J, Zaninovic N, Zhan Q, Madireddy A, Nolin SL, Ersalesi N, Yan Z, Rosenwaks Z, Schildkraut CL.
Gerhardt J, et al. Among authors: ersalesi n.
J Cell Biol. 2014 Sep 1;206(5):599-607. doi: 10.1083/jcb.201404157.
J Cell Biol. 2014.
PMID: 25179629
Free PMC article.
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