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Inherited deletion at Duchenne dystrophy locus in normal male.
Koh J, Bartlett RJ, Pericak-Vance MA, Speer MC, Yamaoka LH, Phillips K, Hung WY, Ray PN, Worton RG, Gilbert JR, et al. Koh J, et al. Among authors: yamaoka lh. Lancet. 1987 Nov 14;2(8568):1154-5. doi: 10.1016/s0140-6736(87)91590-x. Lancet. 1987. PMID: 2890056 No abstract available.
Inherited deletion at Duchenne dystrophy locus in normal male.
Bartlett RJ, Walker AP, Laing NG, Koh J, Secore SL, Speer MC, Pericak-Vance M, Hung WY, Yamaoka LH, Siddique T, et al. Bartlett RJ, et al. Among authors: yamaoka lh. Lancet. 1989 Mar 4;1(8636):496-7. doi: 10.1016/s0140-6736(89)91394-9. Lancet. 1989. PMID: 2563864 No abstract available.
Duchenne muscular dystrophy: high frequency of deletions.
Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka LH, Chen JC, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJ, Bakker E, et al. Bartlett RJ, et al. Among authors: yamaoka lh. Neurology. 1988 Jan;38(1):1-4. doi: 10.1212/wnl.38.1.1. Neurology. 1988. PMID: 3275902
RFLP for Duchenne muscular dystrophy cDNA clone 44-1.
Laing NG, Siddique T, Bartlett RJ, Yamaoka LH, Chen JC, Walker AP, Hung WY, Roses AD. Laing NG, et al. Among authors: yamaoka lh. Nucleic Acids Res. 1988 Jul 25;16(14B):7209. doi: 10.1093/nar/16.14.7209. Nucleic Acids Res. 1988. PMID: 2900496 Free PMC article.
RFLP for Duchenne muscular dystrophy cDNA clone 30-2.
Walker AP, Bartlett RJ, Laing NG, Siddique T, Yamaoka LH, Chen JC, Hung WY, Roses AD. Walker AP, et al. Among authors: yamaoka lh. Nucleic Acids Res. 1988 Sep 26;16(18):9072. doi: 10.1093/nar/16.18.9072. Nucleic Acids Res. 1988. PMID: 2902573 Free PMC article. No abstract available.
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).
Gilbert JR, Stajich JM, Speer MC, Vance JM, Stewart CS, Yamaoka LH, Samson F, Fardeau M, Potter TG, Roses AD, et al. Gilbert JR, et al. Among authors: yamaoka lh. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.
57 results