Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD) by GILBERT, J. R, STAJICH, J. M, ROZEAR, M, SAMSON, F, FARDEAU, M, ROSES, A. D, PERICAK-VANCE, M. A, WALL, S, CARTER, S. C, QIU, H, VANCE, J. M, STEWART, C. S, SPEER, M. C, PUFKY, J, YAMAOKA, L. H

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Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B by Vance, J M, Speer, M C, Stajich, J M, West, S, Wolpert, C, Gaskell, P, Lennon, F, Tim, R M, Rozear, M, Othmane, K B

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Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity by Pericak-Vance, M A, Speer, M C, Lennon, F, West, S G, Menold, M M, Stajich, J M, Wolpert, C M, Slotterbeck, B D, Saito, M, Tim, R W, Rozear, M P, Middleton, L T, Tsuji, S, Vance, J M

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Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B by Gilbert, J R, Speer, M C, Stajich, J, Clancy, R, Lewis, K, Qiu, H, Yamaoka, L, Kumar, A, Vance, J, Stewart, C, Rozear, M, Roses, A D, Pericak-Vance, M A

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Factors associated with survival in the National Registry of Veterans with ALS by Pastula, Daniel M., Coffman, Cynthia J., Allen, Kelli D., Oddone, Eugene Z., Kasarskis, Edward J., Lindquist, Jennifer H., Morgenlander, Joel C., Norman, Barbara B., Rozear, Marvin P., Sams, Laura A., Sabet, Arman, Bedlack, Richard S.

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READER OPINIONS by Weber, John R, Dennis, Ron, Matthews, John, Mckinney, Larry, Hilburn, Darlene, Reid, Jason, Banks, Bobbie Wrenn, Iskander, John, Silverman, Alida C, Thomson, Dick

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