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Scott, WK
Nance, MA
Watts, RL
Hubble, JP
Koller, WC
Lyons, K
Pahwa, R
Stern, MB
Colcher, A
Hiner, BC
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Ondo, WG
Allen, FH
Goetz, CG
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Masterman, D
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Laing, NG
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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
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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:
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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
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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
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