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Page 1
Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis.
Feldmann D, Denoyelle F, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Le Maréchal C, Dollfus H, Eliot MM, Delaunoy JP, David A, Calais C, Drouin-Garraud V, Obstoy MF, Bouccara D, Sterkers O, Huy PT, Goizet C, Duriez F, Fellmann F, Hélias J, Vigneron J, Montaut B, Lewin P, Petit C, Marlin S. Feldmann D, et al. Among authors: petit c. Am J Med Genet A. 2004 Jun 15;127A(3):263-7. doi: 10.1002/ajmg.a.20588. Am J Med Genet A. 2004. PMID: 15150777
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
Denoyelle F, Weil D, Maw MA, Wilcox SA, Lench NJ, Allen-Powell DR, Osborn AH, Dahl HH, Middleton A, Houseman MJ, Dodé C, Marlin S, Boulila-ElGaïed A, Grati M, Ayadi H, BenArab S, Bitoun P, Lina-Granade G, Godet J, Mustapha M, Loiselet J, El-Zir E, Aubois A, Joannard A, Levilliers J, Garabédian EN, Mueller RF, Gardner RJ, Petit C, et al. Denoyelle F, et al. Among authors: petit c. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442
A particular case of deafness-oligodontia syndrome.
Marlin S, Denoyelle F, Busquet D, Garabedian N, Petit C. Marlin S, et al. Among authors: petit c. Int J Pediatr Otorhinolaryngol. 1998 Jun 1;44(1):63-9. doi: 10.1016/s0165-5876(98)00029-9. Int J Pediatr Otorhinolaryngol. 1998. PMID: 9720683
[Hereditary sensorineural deafness].
Denoyelle F, Marlin S, Petit C, Garabédian EN. Denoyelle F, et al. Among authors: petit c. Rev Prat. 2000 Jan 15;50(2):146-9. Rev Prat. 2000. PMID: 10737085 French.
DFNA3.
Denoyelle F, Weil D, Levilliers J, Petit C. Denoyelle F, et al. Among authors: petit c. Adv Otorhinolaryngol. 2000;56:78-83. doi: 10.1159/000059086. Adv Otorhinolaryngol. 2000. PMID: 10868217 Review. No abstract available.
1,067 results