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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: schwartz ce. Am J Hum Genet. 2000 Feb;66(2):480-93. doi: 10.1086/302762. Am J Hum Genet. 2000. PMID: 10677308 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: schwartz ce. Am J Hum Genet. 1998 Sep;63(3):776-85. doi: 10.1086/302018. Am J Hum Genet. 1998. PMID: 9718348 Free PMC article.
Renpenning syndrome maps to Xp11.
Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE. Stevenson RE, et al. Among authors: schwartz ce. Am J Hum Genet. 1998 May;62(5):1092-101. doi: 10.1086/301835. Am J Hum Genet. 1998. PMID: 9545405 Free PMC article.
532 results