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Aneuploidy and the fragile X syndrome.
Watson MS, Breg WR, Pauls D, Brown WT, Carroll AJ, Howard-Peebles PN, Meryash D, Shapiro LR. Watson MS, et al. Am J Med Genet. 1988 May-Jun;30(1-2):115-21. doi: 10.1002/ajmg.1320300110. Am J Med Genet. 1988. PMID: 2972203
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: howard peebles pn. Am J Hum Genet. 2000 Feb;66(2):480-93. doi: 10.1086/302762. Am J Hum Genet. 2000. PMID: 10677308 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: howard peebles pn. Am J Med Genet. 1999 Apr 2;83(4):322-5. Am J Med Genet. 1999. PMID: 10208170 Free PMC article.
98 results