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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: davies ke. Am J Hum Genet. 1990 Aug;47(2):181-6. Am J Hum Genet. 1990. PMID: 2378345 Free PMC article.
Physical mapping of DXS134 close to the DXS52 locus.
Bell MV, Patterson MN, Dorkins HR, Davies KE. Bell MV, et al. Among authors: davies ke. Hum Genet. 1989 Apr;82(1):27-30. doi: 10.1007/BF00288266. Hum Genet. 1989. PMID: 2565864
Linkage studies in a large fragile X family.
Patterson M, Bell M, Kress W, Davies KE, Froster-Iskenius U. Patterson M, et al. Among authors: davies ke. Am J Hum Genet. 1988 Nov;43(5):684-8. Am J Hum Genet. 1988. PMID: 2903666 Free PMC article.
Molecular analysis of the fragile X syndrome.
Froster-Iskenius U, Patterson MN, Bell MV, Bloomfield J, Davies KE. Froster-Iskenius U, et al. Among authors: davies ke. Q J Med. 1988 Oct;68(258):755-63. Q J Med. 1988. PMID: 3077469 Review. No abstract available.
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: davies ke. 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.
2,551 results