Authors: Mansour, I Delague, V Cazeneuve, C Dode, C Chouery, E Pecheux, C Medlej-Hashim, M Salem, N El Zein, L Levan-Petit, I Lefranc, G Goossens, M Delpech, M Amselem, S Loiselet, J Grateau, G Megarbane, A Naman, R

Citation: I. Mansour et al., Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Creek orthodoxes, Creek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M6941 mutations, EUR J HUM G, 9(1), 2001, pp. 51-55

Authors: Delague, V Bareil, C Bouvagnet, P Salem, N Chouery, E Loiselet, J Megarbane, A Claustres, M

Citation: V. Delague et al., Nonprogressive autosomal recessive ataxia maps to chromosome 9q34-9qter ina large consanguineous Lebanese family, ANN NEUROL, 50(2), 2001, pp. 250-253

Authors: Megarbane, A Waked, N Chouery, E Moglabey, YB Saliba, N Mornet, E Serre, JL Slim, R

Citation: A. Megarbane et al., Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers, AM J MED G, 98(3), 2001, pp. 244-249

Authors: Delague, V Souraty, N Khallouf, E Tardy, V Chouery, E Halaby, G Loiselet, J Morel, Y Megarbane, A

Citation: V. Delague et al., Mutational analysis in Lebanese patients with congenital adrenal hyperplasia due to a deficit in 21-hydroxylase, HORMONE RES, 53(2), 2000, pp. 77-82

Authors: Delague, V Bareil, C Tuffery, S Bouvagnet, P Chouery, E Koussa, S Maisonobe, T Loiselet, J Megarbane, A Claustres, M

Citation: V. Delague et al., Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: Exclusion of MAG as a candidate gene, AM J HU GEN, 67(1), 2000, pp. 236-243