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Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.
Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, Juncos J, Nelson DL, Epstein MP, Cutler DJ, Todd PK, Sherman SL, Warren ST, Jin P. Kong HE, et al. Among authors: sherman sl. Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2118124119. doi: 10.1073/pnas.2118124119. Epub 2022 May 26. Proc Natl Acad Sci U S A. 2022. PMID: 35617426 Free PMC article.
An n-allele model for progressive amplification in the FMR1 locus.
Morris A, Morton NE, Collins A, Macpherson J, Nelson D, Sherman S. Morris A, et al. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4833-7. doi: 10.1073/pnas.92.11.4833. Proc Natl Acad Sci U S A. 1995. PMID: 7761409 Free PMC article.
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 Free PMC article.
Prevalence of the fragile X syndrome in African-Americans.
Crawford DC, Meadows KL, Newman JL, Taft LF, Scott E, Leslie M, Shubek L, Holmgreen P, Yeargin-Allsopp M, Boyle C, Sherman SL. Crawford DC, et al. Among authors: sherman sl. Am J Med Genet. 2002 Jul 1;110(3):226-33. doi: 10.1002/ajmg.10427. Am J Med Genet. 2002. PMID: 12116230
430 results