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Results: 1-6 |
Results: 6

Authors: Bell, R Brice, G Child, AH Murday, VA Mansour, S Sandy, CJ Collin, JRO Brady, AF Callen, DF Burnand, K Mortimer, P Jeffery, S
Citation: R. Bell et al., Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene, HUM GENET, 108(6), 2001, pp. 546-551

Authors: Lai, SH Goldman, JA Child, AH Engel, A Lamm, SH
Citation: Sh. Lai et al., Fibromyalgia, hypermobility, and breast implants, J RHEUMATOL, 27(9), 2000, pp. 2237-2241

Authors: Bell, R Brice, G Child, AH Murday, VA Mansour, S Sandy, CJ Collin, JRO Mortimer, P Callen, DF Burnand, K Jeffery, S
Citation: R. Bell et al., Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb, J MED GENET, 37(9), 2000, pp. 725-726

Authors: Rosbotham, JL Brice, GW Child, AH Nunan, TO Mortimer, PS Burnand, KG
Citation: Jl. Rosbotham et al., Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy, BR J DERM, 142(1), 2000, pp. 148-152

Authors: Child, AH Beninson, J Sarfarazi, M
Citation: Ah. Child et al., Cause of primary congenital lymphedema - Commentary, ANGIOLOGY, 50(4), 1999, pp. 325-326

Authors: Mangion, J Rahman, N Mansour, S Brice, G Rosbotham, J Child, AH Murday, VA Mortimer, PS Barfoot, R Sigurdsson, A Edkins, S Sarfarazi, M Burnand, K Evans, AL Nunan, TO Stratton, MR Jeffery, S
Citation: J. Mangion et al., A gene for lymphedema-distichiasis maps to 16q24.3, AM J HU GEN, 65(2), 1999, pp. 427-432
Risultati: 1-6 |