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Page 1
Investigation of the PARK10 gene in Parkinson disease.
Li YJ, Deng J, Mayhew GM, Grimsley JW, Huo X, Vance JM. Li YJ, et al. Among authors: vance jm. Ann Hum Genet. 2007 Sep;71(Pt 5):639-47. doi: 10.1111/j.1469-1809.2007.00353.x. Epub 2007 Mar 27. Ann Hum Genet. 2007. PMID: 17388942
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.
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.
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.
Speer MC, Tandan R, Rao PN, Fries T, Stajich JM, Bolhuis PA, Jöbsis GJ, Vance JM, Viles KD, Sheffield K, James C, Kahler SG, Pettenati M, Gilbert JR, Denton PH, Yamaoka LH, Pericak-Vance MA. Speer MC, et al. Among authors: vance jm. Hum Mol Genet. 1996 Jul;5(7):1043-6. doi: 10.1093/hmg/5.7.1043. Hum Mol Genet. 1996. PMID: 8817344
307 results