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Fragile X syndrome without CCG amplification has an FMR1 deletion.
Gedeon AK, Baker E, Robinson H, Partington MW, Gross B, Manca A, Korn B, Poustka A, Yu S, Sutherland GR, et al. Gedeon AK, et al. Among authors: yu s. Nat Genet. 1992 Aug;1(5):341-4. doi: 10.1038/ng0892-341. Nat Genet. 1992. PMID: 1302032
Experience with direct molecular diagnosis of fragile X.
Mulley JC, Yu S, Gedeon AK, Donnelly A, Turner G, Loesch D, Chapman CJ, Gardner RJ, Richards RI, Sutherland GR. Mulley JC, et al. Among authors: yu s. J Med Genet. 1992 Jun;29(6):368-74. doi: 10.1136/jmg.29.6.368. J Med Genet. 1992. PMID: 1619631 Free PMC article.
Isolation of a human DNA sequence which spans the fragile X.
Kremer EJ, Yu S, Pritchard M, Nagaraja R, Heitz D, Lynch M, Baker E, Hyland VJ, Little RD, Wada M, et al. Kremer EJ, et al. Among authors: yu s. Am J Hum Genet. 1991 Sep;49(3):656-61. Am J Hum Genet. 1991. PMID: 1882843 Free PMC article.
Fragile X genotype characterized by an unstable region of DNA.
Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Yu S, et al. Science. 1991 May 24;252(5009):1179-81. doi: 10.1126/science.252.5009.1179. Science. 1991. PMID: 2031189
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