Petit C - Search Results

1

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.

2

Genes responsible for human hereditary deafness: symphony of a thousand.

Petit C. Petit C. Nat Genet. 1996 Dec;14(4):385-91. doi: 10.1038/ng1296-385. Nat Genet. 1996. PMID: 8944017 Review.

3

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

4

Connexin 26 gene linked to a dominant deafness.

Denoyelle F, Lina-Granade G, Plauchu H, Bruzzone R, Chaïb H, Lévi-Acobas F, Weil D, Petit C. Denoyelle F, et al. Among authors: petit c. Nature. 1998 May 28;393(6683):319-20. doi: 10.1038/30639. Nature. 1998. PMID: 9620796 No abstract available.

5

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

6

[Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people].

Marlin S, Denoyelle F, Garabédian EN, Petit C. Marlin S, et al. Among authors: petit c. Ann Otolaryngol Chir Cervicofac. 1998 Feb;115(1):3-8. Ann Otolaryngol Chir Cervicofac. 1998. PMID: 9765703 French.

7

Two cases of Townes-Brocks syndrome with previously undescribed anomalies.

Marlin S, Toublanc JE, Petit C. Marlin S, et al. Among authors: petit c. Clin Dysmorphol. 1998 Oct;7(4):295-8. doi: 10.1097/00019605-199810000-00011. Clin Dysmorphol. 1998. PMID: 9823498

8

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.

Kubisch C, Schroeder BC, Friedrich T, Lütjohann B, El-Amraoui A, Marlin S, Petit C, Jentsch TJ. Kubisch C, et al. Among authors: petit c. Cell. 1999 Feb 5;96(3):437-46. doi: 10.1016/s0092-8674(00)80556-5. Cell. 1999. PMID: 10025409 Free article.

9

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

Denoyelle F, Marlin S, Weil D, Moatti L, Chauvin P, Garabédian EN, Petit C. Denoyelle F, et al. Among authors: petit c. Lancet. 1999 Apr 17;353(9161):1298-303. doi: 10.1016/S0140-6736(98)11071-1. Lancet. 1999. PMID: 10218527

10

Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.

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. Marlin S, et al. Among authors: petit c. Hum Mutat. 1999;14(5):377-86. doi: 10.1002/(SICI)1098-1004(199911)14:5<377::AID-HUMU3>3.0.CO;2-A. Hum Mutat. 1999. PMID: 10533063

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