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Results: 1-6 |
Results: 6

Authors: Scott, WK Nance, MA Watts, RL Hubble, JP Koller, WC Lyons, K Pahwa, R Stern, MB Colcher, A Hiner, BC Jankovic, J Ondo, WG Allen, FH Goetz, CG Small, GW Masterman, D Mastaglia, F Laing, NG Stajich, JM Slotterbeck, B Booze, MW Ribble, RC Rampersaud, E West, SG Gibson, RA Middleton, LT Roses, AD Haines, JL Scott, BL Vance, JM Pericak-Vance, MA
Citation: Wk. Scott et al., Complete genomic screen in parkinson disease - Evidence for multiple genes, J AM MED A, 286(18), 2001, pp. 2239-2244

Authors: Martin, ER Scott, WK Nance, MA Watts, RL Hubble, JP Koller, WC Lyons, K Pahwa, R Stern, MB Colcher, A Hiner, BC Jankovic, J Ondo, WG Allen, FH Goetz, CG Small, GW Masterman, D Mastaglia, F Laing, NG Stajich, JM Ribble, RC Booze, MW Rogala, A Hauser, MA Zhang, FY Gibson, RA Middleton, LT Roses, AD Haines, JL Scott, BL Pericak-Vance, MA Vance, JM
Citation: Er. Martin et al., Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease, J AM MED A, 286(18), 2001, pp. 2245-2250

Authors: Hauser, MA Horrigan, SK Salmikangas, P Torian, UM Viles, KD Dancel, R Tim, RW Taivainen, A Bartoloni, L Gilchrist, JM Stajich, JM Gaskell, PC Gilbert, JR Vance, JM Pericak-Vance, MA Carpen, O Westbrook, CA Speer, MC
Citation: Ma. Hauser et al., Myotilin is mutated in limb girdle muscular dystrophy 1A, HUM MOL GEN, 9(14), 2000, pp. 2141-2147

Authors: Speer, MC Vance, JM Grubber, JM Graham, FL Stajich, JM Viles, KD Rogala, A McMichael, R Chutkow, J Goldsmith, C Tim, RW Pericak-Vance, MA
Citation: Mc. Speer et al., Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7, AM J HU GEN, 64(2), 1999, pp. 556-562

Authors: Alberts, MJ Stajich, JM
Citation: Mj. Alberts et Jm. Stajich, Evaluation of stroke patients for inherited causes of stroke, GENETICS OF CEREBROVASCULAR DISEASE, 1999, pp. 335-344

Authors: Bartoloni, L Horrigan, SK Viles, KD Gilchrist, JM Stajich, JM Vance, JM Yamaoka, LH Pericak-Vance, MA Westbrook, CA Speer, MC
Citation: L. Bartoloni et al., Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31, GENOMICS, 54(2), 1998, pp. 250-255
Risultati: 1-6 |