Browsing Centre for Genomics and Child Health by Author "Dafou, D"
Now showing items 1-3 of 3
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Dymeclin, the Gene Underlying Dyggve-Melchior-Clausen Syndrome, Encodes a Protein Integral to Extracellular Matrix and Golgi Organization and is Associated with Protein Secretion Pathways Critical in Bone Development
Denais, C; Dent, CL; Southgate, L; Hoyle, J; Dafou, D; Trembath, RC; Machado, RD (2011-02) -
Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies
Southgate, L; Machado, RD; Snape, KM; Primeau, M; Dafou, D; Ruddy, DM; Branney, PA; Fisher, M; Lee, GJ; Simpson, MA (2011-05-13) -
Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish
Southgate, L; Dafou, D; Hoyle, J; Li, N; Kinning, E; Critchley, P; Nemeth, AH; Talbot, K; Bindu, PS; Sinha, S (2010-10)