Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity von Othmane, Kamel Ben, Middleton, Lefkos T., Loprest, Lorraine J., Wilkinson, Kenneth M., Lennon, Felicia, Rozear, Marvin P., Stajich, Jeffrey U., Gaskell, Perry C., Roses, Allen D., Pericak-Vance, Margaret A., Vance, Jeffery M.

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Myotilin is mutated in limb girdle muscular dystrophy 1A von HAUSER, M. A, HORRIGAN, S. K, STAJICH, J. M, GASKELL, P. C, GILBERT, J. R, VANCE, J. M, PERICAK-VANCE, M. A, CARPEN, O, WESTBROOK, C. A, SPEER, M. C, SALMIKANGAS, P, TORIAN, U. M, VILES, K. D, DANCEL, R, TIM, R. W, TAIVAINEN, A, BARTOLONI, L, GILCHRIST, J. M

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Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2 von Vance, Jeffery M., Barker, David, Yamaoka, Larry H., Stajich, Jeffrey M., Loprest, Lorraine, Hung, Wu-Yen, Fischbeck, Kenneth, Roses, Allen D., Pericak-Vance, Margaret A.

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IDENTIFICATION OF GENETIC MARKERS ASSOCIATED WITH PARKINSON DISEASE von STAJICH JEFFREY M, WALT JOELLE VAN DER, LI YI-JU, SCOTT WILLIAM K, OLIVEIRA SOFIA, PERICAK-VANCE MARGARET A, VANCE JEFFERY M, MARTIN EDEN R, HAUSER MICHAEL A

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Identification of genetic markers associated with parkinson disease von STAJICH JEFFREY M, WALT JOELLE VAN DER, LI YI-JU, SCOTT WILLIAM K, OLIVEIRA SOFIA, PERICAK-VANCE MARGARET A, VANCE JEFFERY M, MARTIN EDEN R, HAUSER MICHAEL A

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