A mutation at codon 279 (N279k) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy von DELISLE, M.-B, MURRELL, J. R, RICHARDSON, R, TROFATTER, J. A, RASCOL, O, SOULAGES, X, MOHR, M, CALVAS, P, GHETTI, B

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Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types von Gusella, James F, Ramesh, Vijaya, Menon, Anil G, Morin, Francine, Hara, Tetsuo, Bianchi, Albert B, Klein-Szanto, Andrés J. P, Gao, Jizong, Trofatter, James A, Kley, Nikolai, Seizinger, Bernd R

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Suicide risk in Huntington's disease von Di Maio, L, Squitieri, F, Napolitano, G, Campanella, G, Trofatter, J A, Conneally, P M

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Isolation of genes from complex sources of mammalian genomic DNA using exon amplification von Church, Deanna M, Stotler, Christy J, Rutter, Joni L, Murrell, Jill R, Trofatter, James A, Buckler, Alan J

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New Quantitative Trait Loci for the Genetic Variance in Circadian Period of Locomotor Activity between Inbred Strains of Mice von Hofstetter, J. R., Trofatter, J. A., Nurnberger, J. I., Kernek, K. L., Mayeda, A. R.

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Exon scanning for mutation of the NF2 gene in schwannomas von Jacoby, Lee B., MacCollin, Mia, Louls, David N., Mohney, Trina, Rublo, Mari-Paz, Pulaski, Karen, Trofatter, James A., Kley, Nikolai, Seizinger, Bernd, Ramesh, Vijaya, Gusella, James F.

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor von Trofatter, James A., MacCollin, Mia M., Rutter, Joni L., Murrell, Jill R., Duyao, Mabel P., Parry, Dilys M., Eldridge, Roswell, Kley, Nikolai, Menon, Anil G., Pulaski, Karen, Haase, Volker H., Ambrose, Christine M., Munroe, David, Bove, Catherine, Haines, Jonathan L., Martuza, Robert L., MacDonald, Marcy E., Seizinger, Bernd R., Short, M.Priscilla, Buckler, Alan J., Gusella, James F.

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Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene von FONTAINE, B, KHURANA, T. S, ROMANO, D, GUSELLA, J. F, BROWN, R. H, HOFFMAN, E. P, BRUNS, G. A. P, HAINES, J. L, TROFATTER, J. A, HANSON, M. P, RICH, J, MCFARLANE, H, YASEK, D. M

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Pelizaeus-Merzbacher Disease: Tight Linkage to Proteolipid Protein Gene Exon Variant von Trofatter, James A., Dlouhy, Stephen R., DeMyer, William, Conneally, P. Michael, Hodes, M. E.

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Mutational analysis of patients with neurofibromatosis 2 von MACCOLLIN, M, VIJAYA RAMESH, PARRY, D. M, GUSELLA, J. F, JACOBY, L. B, LOUIS, D. N, RUBIO, M.-P, PULASKI, K, TROFATTER, J. A, SHORT, M. P, BOVE, C, ELDRIDGE, R

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor von Trofatter, J A, MacCollin, M M, Rutter, J L, Murrell, J R, Duyao, M P, Parry, D M, Eldridge, R, Kley, N, Menon, A G, Pulaski, K

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Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22 von Rouleau, Guy A, Wertelecki, Wladimir, Haines, Jonathan L, Hobbs, Wendy J, Trofatter, James A, Seizinger, Bernd R, Martuza, Robert L, Superneau, Duane W, Conneally, P. Michael, Gusella, James F

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Onset symptoms in 510 patients with Huntington's disease von Di Maio, L, Squitieri, F, Napolitano, G, Campanella, G, Trofatter, J A, Conneally, P M

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Cloning and Characterization of a Novel Human Clathrin Heavy Chain Gene (CLTCL) von Long, Kimberly R., Trofatter, James A., Ramesh, Vijaya, McCormick, Mary Kay, Buckler, Alan J.

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Myelin Protein Zero Gene Mutated in Charcot-Marie-Tooth Type 1B Patients von Su, Ying, Brooks, David G., Li, Lanying, Lepercq, Jacques, Trofatter, James A., Ravetch, Jeffrey V., Lebo, Roger V.

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Genetic linkage studies in Alzheimer's disease families von Pericak-Vance, M.A., Yamaoka, L.H., Haynes, C.S., Speer, M.C., Haines, J.L., Gaskell, P.C., Hung, W.-Y., Clark, C.M., Heyman, A.L., Trofatter, J.A., Eisenmenger, J.P., Gilbert, J.R., Lee, J.E., Alberts, M.J., Dawson, D.V., Bartlett, R.J., Earl, N.L., Siddique, T., Vance, J.M., Conneall, P.M., Roses, A.D.

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The murine NF2 homologue encodes a highly conserved merlin protein with alternative forms von Haase, Volker H., Trofatter, James A., MacCollin, Mla, Tarttelln, Emma, Gusella, James F., Ramesh, Vijaya

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Dinucleotide repeat polymorphism at the debrisoquine 4-hydroxylase (CYP2D) locus von TROFATTER, J. A, GUSELLA, J. F, HAINES, J. L

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Transducer Choice Questioned von Trofatter, John

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Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma von Seizinger, B. R, Rouleau, G. A, Ozelius, L. J, Lane, A. H, Farmer, G. E, Lamiell, J. M, Haines, J, Yuen, J. W. M, Collins, D, Majoor-Krakauer, D, Bonner, T, Mathew, C, Rubenstein, A, Halperin, J, McConkie-Rosell, A, Green, J. S, Trofatter, J. A, Ponder, B. A, Eierman, L, Bowmer, M. I, Schimke, R, Oostra, B, Aronin, N, Smith, D. I, Drabkin, H, Waziri, M. H, Hobbs, W. J, Martuza, R. L, Conneally, P. M, Hsia, Y. E, Gusella, J. F

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