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Molecular heterogeneity of the fragile X syndrome.
Nakahori Y, Knight SJ, Holland J, Schwartz C, Roche A, Tarleton J, Wong S, Flint TJ, Froster-Iskenius U, Bentley D, et al. Nakahori Y, et al. Among authors: roche a. Nucleic Acids Res. 1991 Aug 25;19(16):4355-9. doi: 10.1093/nar/19.16.4355. Nucleic Acids Res. 1991. PMID: 1886762 Free PMC article.
Molecular analysis of the fragile X syndrome.
Hirst MC, Knight SM, Nakahori Y, Roche A, Davies KE. Hirst MC, et al. Among authors: roche a. J Inherit Metab Dis. 1992;15(4):532-8. doi: 10.1007/BF01799612. J Inherit Metab Dis. 1992. PMID: 1528014 Review.
Molecular studies of the fragile X syndrome.
Knight SJ, Hirst MC, Roche A, Christodoulou Z, Huson SM, Winter R, Fitchett M, McKinley MJ, Lindenbaum RH, Nakahori Y, et al. Knight SJ, et al. Among authors: roche a. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):217-23. doi: 10.1002/ajmg.1320430135. Am J Med Genet. 1992. PMID: 1605194
Genotype prediction in the fragile X syndrome.
Hirst MC, Nakahori Y, Knight SJ, Schwartz C, Thibodeau SN, Roche A, Flint TJ, Connor JM, Fryns JP, Davies KE. Hirst MC, et al. Among authors: roche a. J Med Genet. 1991 Dec;28(12):824-9. doi: 10.1136/jmg.28.12.824. J Med Genet. 1991. PMID: 1757957 Free PMC article.
A YAC contig across the fragile X site defines the region of fragility.
Hirst MC, Rack K, Nakahori Y, Roche A, Bell MV, Flynn G, Christadoulou Z, MacKinnon RN, Francis M, Littler AJ, et al. Hirst MC, et al. Among authors: roche a. Nucleic Acids Res. 1991 Jun 25;19(12):3283-8. doi: 10.1093/nar/19.12.3283. Nucleic Acids Res. 1991. PMID: 2062644 Free PMC article.
Primary structure of dystrophin-related protein.
Tinsley JM, Blake DJ, Roche A, Fairbrother U, Riss J, Byth BC, Knight AE, Kendrick-Jones J, Suthers GK, Love DR, et al. Tinsley JM, et al. Among authors: roche a. Nature. 1992 Dec 10;360(6404):591-3. doi: 10.1038/360591a0. Nature. 1992. PMID: 1461283
1,240 results