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Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.
Kaufmann WE, Kidd SA, Andrews HF, Budimirovic DB, Esler A, Haas-Givler B, Stackhouse T, Riley C, Peacock G, Sherman SL , Brown WT, Berry-Kravis E.
Kaufmann WE, et al. Among authors: sherman sl .
Pediatrics. 2017 Jun;139(Suppl 3):S194-S206. doi: 10.1542/peds.2016-1159F.
Pediatrics. 2017.
PMID: 28814540
Free PMC article.
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Collaborative prospective study of the fragile X syndrome: one-year progress report.
Sherman SL , Barbi G, Brøndum-Nielsen K, Brown WT, Carpenter NJ, Chudley AE, Ferraz OP, Ferreira P, Gustavson KH, Halliday J, et al.
Sherman SL , et al.
Am J Med Genet. 1992 Apr 15-May 1;43(1-2):355-60. doi: 10.1002/ajmg.1320430155.
Am J Med Genet. 1992.
PMID: 1605212
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Laboratory aspects of prenatal fra(X) detection.
Jenkins EC, Krawczun MS, Brooks SE, Brooks SL, Sherman SL , Brown WT.
Jenkins EC, et al. Among authors: sherman sl .
Prog Clin Biol Res. 1991;368:27-42.
Prog Clin Biol Res. 1991.
PMID: 1835094
No abstract available.
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Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses.
Sherman SL , Maddalena A, Howard-Peebles PN, Brown WT, Nolin S, Jenkins E, Schwartz C, Tarrelton J, Shapiro LR, Smits AP, et al.
Sherman SL , et al.
Am J Med Genet. 1994 Jul 15;51(4):503-6. doi: 10.1002/ajmg.1320510442.
Am J Med Genet. 1994.
PMID: 7943029
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Seventh International Workshop on the Fragile X and X-linked Mental Retardation.
Tranebjaerg L, Lubs HA, Borghgraef M, Brown WT, Fisch G, Fryns JP, Hagerman R, Jacobs PA, Mandel JL, Mulley J, Oostra B, Schwartz C, Sherman S, Willard H, Willems P.
Tranebjaerg L, et al.
Am J Med Genet. 1996 Jul 12;64(1):1-14. doi: 10.1002/(SICI)1096-8628(19960712)64:1<1::AID-AJMG1>3.0.CO;2-Z.
Am J Med Genet. 1996.
PMID: 8826442
No abstract available.
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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: sherman sl .
Am J Hum Genet. 1996 Dec;59(6):1252-61.
Am J Hum Genet. 1996.
PMID: 8940270
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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: sherman sl .
Am J Hum Genet. 2000 Feb;66(2):480-93. doi: 10.1086/302762.
Am J Hum Genet. 2000.
PMID: 10677308
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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. Among authors: sherman sl .
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.
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