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Results: 1-5 |
Results: 5

Authors: Zhao, XP Alvarado, D Rainier, S Lemons, R Hedera, P Weber, CH Tukel, T Apak, M Heiman-Patterson, T Ming, L Bui, M Fink, JK
Citation: Xp. Zhao et al., Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia, NAT GENET, 29(3), 2001, pp. 326-331

Authors: Grunder, S Geisler, HS Rainier, S Fink, JK
Citation: S. Grunder et al., Acid-sensing ion channel (ASCI) 4 gene: physical mapping, genomic organisation, and evaluation as a candidate for paroxysmal dystonia, EUR J HUM G, 9(9), 2001, pp. 672-676

Authors: Hedera, P Williamson, JA Rainier, S Alvarado, D Tukel, T Apak, M Fink, JK
Citation: P. Hedera et al., Prenatal diagnosis of hereditary spastic paraplegia, PRENAT DIAG, 21(3), 2001, pp. 202-206

Authors: Smith, MJ Gitlin, SD Browning, CM Lane, BR Clark, NM Shah, N Rainier, S Markovitz, DM
Citation: Mj. Smith et al., GLI-2 modulates retroviral gene expression, J VIROLOGY, 75(5), 2001, pp. 2301-2313

Authors: Hedera, P Rainier, S Alvarado, D Zhao, XP Williamson, J Otterud, B Leppert, M Fink, JK
Citation: P. Hedera et al., Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q, AM J HU GEN, 64(2), 1999, pp. 563-569
Risultati: 1-5 |