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Molecular analysis of muscular dystrophy.
Davies KE, Kenwrick SJ, Patterson MN, Smith TJ, Forrest SM, Dorkins HR, Cross GS, England SB. Davies KE, et al. Among authors: patterson mn. J Muscle Res Cell Motil. 1988 Feb;9(1):1-8. doi: 10.1007/BF01682143. J Muscle Res Cell Motil. 1988. PMID: 3292577 Review.
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: patterson mn. Q J Med. 1988 Oct;68(258):755-63. Q J Med. 1988. PMID: 3077469 Review. No abstract available.
Molecular analysis of human muscular dystrophies.
Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M. Davies KE, et al. Muscle Nerve. 1987 Mar-Apr;10(3):191-9. doi: 10.1002/mus.880100302. Muscle Nerve. 1987. PMID: 2882417 Review.
Physical mapping of DXS134 close to the DXS52 locus.
Bell MV, Patterson MN, Dorkins HR, Davies KE. Bell MV, et al. Among authors: patterson mn. Hum Genet. 1989 Apr;82(1):27-30. doi: 10.1007/BF00288266. Hum Genet. 1989. PMID: 2565864
Molecular analysis of X-linked diseases.
Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, Patterson MN, Smith TJ, Old JM, King AW, Thakker RV, et al. Davies KE, et al. Among authors: patterson mn. Ann Clin Res. 1986;18(5-6):231-3. Ann Clin Res. 1986. PMID: 2882726 No abstract available.
Molecular analysis of human X-linked diseases.
Davies KE, Ball SP, Dorkins HR, Forrest SM, Kenwrick SJ, King AW, Lavenir IJ, McGlade SA, Patterson MN, Smith TJ, et al. Davies KE, et al. Among authors: patterson mn. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:337-43. doi: 10.1101/sqb.1986.051.01.039. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3472730 No abstract available.
Linkage studies in a large fragile X family.
Patterson M, Bell M, Kress W, Davies KE, Froster-Iskenius U. Patterson M, et al. Am J Hum Genet. 1988 Nov;43(5):684-8. Am J Hum Genet. 1988. PMID: 2903666 Free PMC article.
41 results