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The fragile X syndrome.
Hirst MC, Knight SJ, Bell MV, Super M, Davies KE. Hirst MC, et al. Among authors: knight sj. Clin Sci (Lond). 1992 Sep;83(3):255-64. doi: 10.1042/cs0830255. Clin Sci (Lond). 1992. PMID: 1327643
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. 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: knight sj. 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.
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: knight sj. 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.
The fragile X syndrome.
Flannery AV, Hirst MC, Knight SJ, Ritchie RJ, Davies KE. Flannery AV, et al. Among authors: knight sj. Biochim Biophys Acta. 1995 Jun 9;1271(2-3):293-303. doi: 10.1016/0925-4439(95)00046-7. Biochim Biophys Acta. 1995. PMID: 7605796 Free article. Review. No abstract available.
Origins of the fragile X syndrome mutation.
Hirst MC, Knight SJ, Christodoulou Z, Grewal PK, Fryns JP, Davies KE. Hirst MC, et al. Among authors: knight sj. J Med Genet. 1993 Aug;30(8):647-50. doi: 10.1136/jmg.30.8.647. J Med Genet. 1993. PMID: 8411050 Free PMC article.
240 results