AAAAAA

   
Results: 1-4 |
Results: 4

Authors: Huber, C Cusin, V Le Merrer, M Mathieu, M Sulmont, V Dagoneau, N Munnich, A Cormier-Daire, V
Citation: C. Huber et al., SHOX point mutations in dyschondrosteosis, J MED GENET, 38(5), 2001, pp. 323-323

Authors: Faivre, L Prieur, AM Le Merrer, M Hayem, F Penet, C Woo, P Hofer, M Dagoneau, N Sermet, I Munnich, A Cormier-Daire, V
Citation: L. Faivre et al., Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome, AM J MED G, 95(3), 2000, pp. 233-236

Authors: Xavier, ABCF Saraiva, JM Le Merrer, M Dagoneau, N Huber, C Penet, C Munnich, A Cormier-Daire, V
Citation: Abcf. Xavier et al., Genetic homogeneity of the Camurati-Engelmann disease, CLIN GENET, 58(2), 2000, pp. 150-152

Authors: Cormier-Daire, V Dagoneau, N Nabbout, R Burglen, L Penet, C Soufflet, C Desguerre, I Munnich, A Dulac, O
Citation: V. Cormier-daire et al., A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31, AM J HU GEN, 67(4), 2000, pp. 991-993
Risultati: 1-4 |