AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Amiel, J Bougeard, G Francannet, C Raclin, V Munnich, A Lyonnet, S Frebourg, T
Citation: J. Amiel et al., TP63 gene mutation in ADULT syndrome, EUR J HUM G, 9(8), 2001, pp. 642-645

Authors: Vanlieferinghen, P Borderon, C Francannet, C Gembara, P Dechelotte, P
Citation: P. Vanlieferinghen et al., Johanson-Blizzard syndrome. A new case with autopsy findings, GEN COUNSEL, 12(3), 2001, pp. 245-250

Authors: Chabrol, B Figarella-Branger, D Coquet, M Mancini, J Fontan, D Pedespan, JM Francannet, C Pouget, J Beaufrere, AM Pellilssier, JF
Citation: B. Chabrol et al., X-linked myopathy with excessive autophagy: a clinicopathological study offive new families, NEUROMUSC D, 11(4), 2001, pp. 376-388

Authors: Benit, P Bonnefont, JP Mostefa, AK Francannet, C Munnich, A Ray, PF
Citation: P. Benit et al., Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis, PRENAT DIAG, 21(4), 2001, pp. 279-283

Authors: Francannet, C Cohen-Tanugi, A Le Merrer, M Munnich, A Bonaventure, J Legeai-Mallet, L
Citation: C. Francannet et al., Genotype-phenotype correlation in hereditary multiple exostoses, J MED GENET, 38(7), 2001, pp. 430-434

Authors: Amiel, J de Lonlay, P Francannet, C Picard, A Bruel, H Rabier, D Le Merrer, M Verhoeven, N Jakobs, C Lyonnet, S Munnich, A
Citation: J. Amiel et al., Facial anomalies in D-2-hydroxyglutaric aciduria, AM J MED G, 86(2), 1999, pp. 124-129
Risultati: 1-6 |