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Citation: S. Marlin et al., Connexin 26 gene mutations in congenitally deaf children - Pitfalls for genetic counseling, ARCH OTOLAR, 127(8), 2001, pp. 927-933

Authors: Norris, B Pritchard, KI James, K Myles, J Bennett, K Marlin, S Skillings, J Findlay, B Vandenberg, T Goss, P Latreille, J Rudinskas, L Lofters, W Trudeau, M Osoba, D Rodgers, A

Citation: B. Norris et al., Phase III comparative study of vinorelbine combined with doxorubicin versus doxorubicin alone in disseminated metastatic/recurrent breast cancer: National Cancer Institute of Canada Clinical Trials Group Study MA8, J CL ONCOL, 18(12), 2000, pp. 2385-2394

Authors: Marlin, S Blanchard, S Slim, R Lacombe, D Denoyelle, F Alessandri, JL Calzolari, E Drouin-Garraud, V Ferraz, FG Fourmaintraux, A Philip, N Toublanc, JE Petit, C

Citation: S. Marlin et al., Townes-Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient, HUM MUTAT, 14(5), 1999, pp. 377-386

Authors: Denoyelle, F Marlin, S Weil, D Moatti, L Chauvin, P Garabedian, EN Petit, C

Citation: F. Denoyelle et al., Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling, LANCET, 353(9161), 1999, pp. 1298-1303

Authors: Kubisch, C Schroeder, BC Friedrich, T Lutjohann, B El-Amraoui, A Marlin, S Petit, C Jentsch, TJ

Citation: C. Kubisch et al., KCNQ4, a novel potassium channel expressed in sensory outer hair cells, ismutated in dominant deafness, CELL, 96(3), 1999, pp. 437-446