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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 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: hirst mc. 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. 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.
Microdissection of the fragile X region.
MacKinnon RN, Hirst MC, Bell MV, Watson JE, Claussen U, Ludecke HJ, Senger G, Horsthemke B, Davies KE. MacKinnon RN, et al. Among authors: hirst mc. Am J Hum Genet. 1990 Aug;47(2):181-6. Am J Hum Genet. 1990. PMID: 2378345 Free PMC article.
The fragile X syndrome.
Hirst MC, Knight SJ, Bell MV, Super M, Davies KE. Hirst MC, et al. Clin Sci (Lond). 1992 Sep;83(3):255-64. doi: 10.1042/cs0830255. Clin Sci (Lond). 1992. PMID: 1327643
51 results