Authors: Colleaux, L Rio, M Heuertz, S Moindrault, S Turleau, C Ozilou, C Gosset, P Raoult, O Lyonnet, S Cormier-Daire, V Amiel, J Le Merrer, M Picq, M de Blois, MC Prieur, M Romana, S Cornelis, F Vekemans, M Munnich, A

Citation: L. Colleaux et al., A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation, EUR J HUM G, 9(5), 2001, pp. 319-327

Authors: Gedeon, AK Tiller, GE Le Merrer, M Heuertz, S Tranebjaerg, L Chitayat, D Robertson, S Glass, IA Savarirayan, R Cole, WG Rimoin, DL Kousseff, BG Ohashi, H Zabel, B Munnich, A Gecz, J Mulley, JC

Citation: Ak. Gedeon et al., The molecular basis of X-linked spondyloepiphyseal dysplasia tarda, AM J HU GEN, 68(6), 2001, pp. 1386-1397

Authors: Aradhya, S Ahobila, P Lewis, RA Nelson, DL Esposito, T Ciccodicola, A Bardaro, T D'Urso, M Woffendin, H Kenwrick, S Smahi, A Heuertz, S Munnich, A Heiss, NS Poustka, A Chishti, AH

Citation: S. Aradhya et al., Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2, AM J MED G, 94(1), 2000, pp. 79-84

Authors: Heiss, NS Poustka, A Knight, SW Aradhya, S Nelson, DL Lewis, RA Esposito, T Ciccodicola, A D'Urso, M Smahi, A Heuertz, S Munnich, A Vabres, P Woffendin, H Kenwrick, S

Citation: Ns. Heiss et al., Mutation analysis of the DKC1 gene in incontinentia pigmenti, J MED GENET, 36(11), 1999, pp. 860-862