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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. Nature. 1992 Dec 10;360(6404):591-3. doi: 10.1038/360591a0. Nature. 1992. PMID: 1461283
Molecular analysis of the fragile X syndrome.
Hirst MC, Knight SM, Nakahori Y, Roche A, Davies KE. Hirst MC, et al. J Inherit Metab Dis. 1992;15(4):532-8. doi: 10.1007/BF01799612. J Inherit Metab Dis. 1992. PMID: 1528014 Review.
Molecular characterization of further dystrophin gene microsatellites.
King SC, Roche AL, Passos-Bueno MR, Takata R, Zatz M, Cockburn DJ, Seller A, Stapleton PM, Love DR. King SC, et al. Among authors: roche al. Mol Cell Probes. 1995 Oct;9(5):361-70. doi: 10.1016/s0890-8508(95)91700-4. Mol Cell Probes. 1995. PMID: 8569778
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. 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. 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.
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. 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.
16 results