Authors:
Corre, A
Chaudre, F
Roger, G
Denoyelle, F
Garabedian, EN
Citation: A. Corre et al., Tracheal dyskinesia associated with midline abnormality: Embryological hypotheses and therapeutic implications, PEDIAT PULM, 2001, pp. 10-12
Authors:
Marlin, S
Garabedian, EN
Roger, G
Moatti, L
Matha, N
Lewin, P
Petit, C
Denoyelle, F
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:
Casademont, I
Chevrier, D
Denoyelle, F
Petit, C
Guesdon, JL
Citation: I. Casademont et al., A simple and reliable method for the detection of the 30delG mutation of the CX26 gene, MOL CELL PR, 14(3), 2000, pp. 149-152
Authors:
Ben Arab, S
Hmani, M
Denoyelle, F
Boulila-Elgaied, A
Chardenoux, S
Hachicha, S
Petit, C
Ayadi, H
Citation: S. Ben Arab et al., Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates, CLIN GENET, 57(6), 2000, pp. 439-443
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