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Myotonic dystrophy: update on progress to define the gene.
Roses AD, Pericak-Vance MA, Bartlett RJ, Yamaoka LH, Lee JE, Koh J, Chen JC, Gilbert JR, Ross DA, Herbstreith MH, et al. Roses AD, et al. Among authors: koh j. Aust Paediatr J. 1988;24 Suppl 1:66-9. Aust Paediatr J. 1988. PMID: 3060077 Review.
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: koh j. Neurology. 1988 Jan;38(1):1-4. doi: 10.1212/wnl.38.1.1. Neurology. 1988. PMID: 3275902
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: koh j. Lancet. 1989 Mar 4;1(8636):496-7. doi: 10.1016/s0140-6736(89)91394-9. Lancet. 1989. PMID: 2563864 No abstract available.
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. Lancet. 1987 Nov 14;2(8568):1154-5. doi: 10.1016/s0140-6736(87)91590-x. Lancet. 1987. PMID: 2890056 No abstract available.
3,103 results