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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: vance jm. Am J Hum Genet. 1992 Aug;51(2):424-7. Am J Hum Genet. 1992. PMID: 1642241 Free PMC article.
Hereditary motor and sensory neuropathies.
Vance JM. Vance JM. J Med Genet. 1991 Jan;28(1):1-5. doi: 10.1136/jmg.28.1.1. J Med Genet. 1991. PMID: 1999826 Free PMC article. Review. No abstract available.
Systematic gene mapping in man: data management considerations.
Pericak-Vance MA, Hung WY, Yamaoka L, Haynes C, Bartlett RJ, Vance JM, Lee J, Siddique T, Gaskell PC, Stajich J, et al. Pericak-Vance MA, et al. Among authors: vance jm. Aust Paediatr J. 1988;24 Suppl 1:87-9. Aust Paediatr J. 1988. PMID: 2904804
Linkage studies in peripheral neurofibromatosis.
Pericak-Vance MA, Yamaoka LH, Vance JM, Aylsworth AS, Rossenwasser GO, Gaskell PC Jr, Alberts MJ, Hung WY, Haynes C, Roses AD. Pericak-Vance MA, et al. Among authors: vance jm. J Med Genet. 1987 Sep;24(9):530-2. doi: 10.1136/jmg.24.9.530. J Med Genet. 1987. PMID: 3118033 Free PMC article.
A novel mutation in the von Hippel-Lindau gene.
Loeb DB, Pericak-Vance MA, Stajich JM, Vance JM. Loeb DB, et al. Among authors: vance jm. Hum Mol Genet. 1994 Aug;3(8):1423-4. doi: 10.1093/hmg/3.8.1423. Hum Mol Genet. 1994. PMID: 7987327 No abstract available.
Dinucleotide repeat polymorphism in the VHL region.
Loeb D, Lui W, Smith DI, Vance JM. Loeb D, et al. Among authors: vance jm. Hum Mol Genet. 1994 Mar;3(3):520. doi: 10.1093/hmg/3.3.520. Hum Mol Genet. 1994. PMID: 8012368 No abstract available.
305 results