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: Malerba, G Lauciello, MC Scherpbier, T Trabetti, E Galavotti, R Cusin, V Pescollderungg, L Zanoni, G Martinati, LC Boner, AL Levitt, RC Pignatti, PF

Citation: G. Malerba et al., Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children, AM J R CRIT, 162(4), 2000, pp. 1587-1590

Authors: Faivre, L Le Merrer, M Megarbane, A Gilbert, B Mortier, G Cusin, V Munnich, A Maroteaux, P Cormier-Daire, V

Citation: L. Faivre et al., Exclusion of chromosome 9 helps to identify mild variants of acromesomelicdysplasia Maroteaux type, J MED GENET, 37(1), 2000, pp. 52-54

Authors: Azancot, A Eydoux, P Vuillard, E Cusin, V Baumann, C Blot, P

Citation: A. Azancot et al., Clinical spectrum of antenatal tetralogy of Fallot., ARCH MAL C, 93(5), 2000, pp. 587-593

Authors: Cormier-Daire, V Belin, V Cusin, V Viot, G Girlich, D Toutain, A Moncla, A Vekemans, M Le Merrer, M Munnich, A

Citation: V. Cormier-daire et al., SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome, ACT PAEDIAT, 88, 1999, pp. 55-59