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Results:
1-7
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Results: 7
Authors:
Reid, E
Escayg, A
Dearlove, AM
Lee, DD
Meisler, MH
Rubinsztein, DC
Citation: E. Reid et al., The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate, J MED GENET, 38(1), 2001, pp. 65-67
Authors:
King, AL
Fraser, JS
Moodle, SJ
Curtis, D
Dearlove, AM
Ellis, HJ
Rosen-Bronson, S
Ciclitira, PJ
Citation: Al. King et al., Coeliac disease: follow-up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11, ANN HUM GEN, 65, 2001, pp. 377-386
Authors:
King, AL
Yiannakou, JY
Brett, PM
Curtis, D
Morris, MA
Dearlove, AM
Rhodes, M
Rosen-Bronson, S
Mathew, C
Ellis, HJ
Ciclitira, PJ
Citation: Al. King et al., A genome-wide family-based linkage study of coeliac disease, ANN HUM GEN, 64, 2000, pp. 479-490
Authors:
Reid, E
Dearlove, AM
Osborn, O
Rogers, MT
Rubinsztein, DC
Citation: E. Reid et al., A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13, AM J HU GEN, 66(2), 2000, pp. 728-732
Authors:
Reid, E
Dearlove, AM
Whiteford, ML
Rhodes, M
Rubinsztein, DC
Citation: E. Reid et al., Autosomal dominant spastic paraplegia - Refined SPG8 locus and additional genetic heterogeneity, NEUROLOGY, 53(8), 1999, pp. 1844-1849
Authors:
Reid, E
Dearlove, AM
Rhodes, M
Rubinsztein, DC
Citation: E. Reid et al., A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity, AM J HU GEN, 65(3), 1999, pp. 757-763
Authors:
Ohadi, M
Lalloz, MRA
Sham, P
Zhao, JH
Dearlove, AM
Shiach, C
Kinsey, S
Rhodes, M
Layton, DM
Citation: M. Ohadi et al., Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping, AM J HU GEN, 64(1), 1999, pp. 165-171
Risultati:
1-7
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