Authors: Flanigan, KM Coffeen, CM Sexton, L Stauffer, D Brunner, S Leppert, MF

Citation: Km. Flanigan et al., Genetic characterization of a large, historically significant Utah kindredwith facioscapulohumeral dystrophy, NEUROMUSC D, 11(6-7), 2001, pp. 525-529

Authors: Howard, MT Shirts, BH Petros, LM Flanigan, KM Gesteland, RF Atkins, JF

Citation: Mt. Howard et al., Sequence specificity of aminoglycoside-induced stop codon readthrough: Potential implications for treatment of Duchenne muscular dystrophy, ANN NEUROL, 48(2), 2000, pp. 164-169

Authors: Flanigan, KM Kerr, M Bromberg, MB Leonard, C Tsuruda, J Zhang, P Gonzalez-Gomez, I Cohn, R Campbell, KP Leppert, M

Citation: Km. Flanigan et al., Congenital muscular dystrophy with rigid spine syndrome: A clinical, pathological, radiological, and genetic study, ANN NEUROL, 47(2), 2000, pp. 152-161

Authors: Plaster, NM Uyama, E Uchino, M Ikeda, T Flanigan, KM Kondo, I Ptacek, LJ

Citation: Nm. Plaster et al., Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24, NEUROLOGY, 53(6), 1999, pp. 1180-1183

Authors: Flanigan, KM Bromberg, MB Gregory, M Baringer, JR Jones, CR Nester, TA Klatt, EC Townsend, JJ

Citation: Km. Flanigan et al., Calciphylaxis mimicking dermatomyositis - Ischemic myopathy complicating renal failure, NEUROLOGY, 51(6), 1998, pp. 1634-1640