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A Bgl II polymorphism detected by LDR152 [D19S19].
Walker AP, Bartlett RJ, Yamaoka LH, Secore SL, Lee JE, Gilbert J, Herbstreith M, Pericak-Vance MA, Hung WY, Roses AD. Walker AP, et al. Among authors: gilbert j. Nucleic Acids Res. 1988 Sep 26;16(18):9063. doi: 10.1093/nar/16.18.9063. Nucleic Acids Res. 1988. PMID: 2902564 Free PMC article.
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. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.
Linkage studies of late-onset familial Alzheimer's disease.
Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Among authors: gilbert jr. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 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. Among authors: gilbert jr. Lancet. 1987 Nov 14;2(8568):1154-5. doi: 10.1016/s0140-6736(87)91590-x. Lancet. 1987. PMID: 2890056 No abstract available.
A new probe for the diagnosis of myotonic muscular dystrophy.
Bartlett RJ, Pericak-Vance MA, Yamaoka L, Gilbert J, Herbstreith M, Hung WY, Lee JE, Mohandas T, Bruns G, Laberge C, et al. Bartlett RJ, et al. Among authors: gilbert j. Science. 1987 Mar 27;235(4796):1648-50. doi: 10.1126/science.3029876. Science. 1987. PMID: 3029876
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: gilbert jr. Aust Paediatr J. 1988;24 Suppl 1:66-9. Aust Paediatr J. 1988. PMID: 3060077 Review.
3,428 results