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Results:
1-8
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Results: 8
Authors:
Dale, RC
Church, AJ
Cardoso, F
Goddard, E
Cox, TC
Chong, WK
Williams, A
Klein, NJ
Neville, BG
Thompson, EJ
Giovannoni, G
Citation: Rc. Dale et al., Poststreptococcal acute disseminated encephalomyelitis with basal ganglia involvement and auto-reactive antibasal ganglia antibodies, ANN NEUROL, 50(5), 2001, pp. 588-595
Authors:
Kirkham, FJ
Calamante, F
Bynevelt, M
Gadian, DG
Evans, JPM
Cox, TC
Connelly, A
Citation: Fj. Kirkham et al., Perfusion magnetic resonance abnormalities in patients with sickle cell disease, ANN NEUROL, 49(4), 2001, pp. 477-485
Authors:
Jensik, PJ
Holbird, D
Collard, MW
Cox, TC
Citation: Pj. Jensik et al., Cloning and characterization of a functional P2X receptor from larval bullfrog skin, AM J P-CELL, 281(3), 2001, pp. C954-C962
Authors:
Kayserili, H
Cox, TC
Cox, LL
Basaran, S
Kilic, G
Ballabio, A
Yuksel-Apak, M
Citation: H. Kayserili et al., Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS), J MED GENET, 38(6), 2001, pp. 411-417
Authors:
Cox, TC
Allen, LR
Cox, LL
Hopwood, B
Goodwin, B
Haan, E
Suthers, GK
Citation: Tc. Cox et al., New mutations in MID1 provide support for loss of function as the cause ofX-linked Opitz syndrome, HUM MOL GEN, 9(17), 2000, pp. 2553-2562
Authors:
Gecz, J
Hillman, MA
Gedeon, AK
Cox, TC
Baker, E
Mulley, JC
Citation: J. Gecz et al., Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tarda, GENOMICS, 69(2), 2000, pp. 242-251
Authors:
Perry, J
Short, KM
Romer, JT
Swift, S
Cox, TC
Ashworth, A
Citation: J. Perry et al., FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules, GENOMICS, 62(3), 1999, pp. 385-394
Authors:
Cox, TC
Citation: Tc. Cox, Calcium and ATP regulation of ion transport in larval frog skin, J COMP PH B, 169(4-5), 1999, pp. 344-350
Risultati:
1-8
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