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213 results

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[Genetic hearing loss].
Tanaka-Ouyang L, Marlin S, Nevoux J. Tanaka-Ouyang L, et al. Among authors: marlin s. Presse Med. 2017 Nov;46(11):1089-1096. doi: 10.1016/j.lpm.2017.09.005. Epub 2017 Oct 28. Presse Med. 2017. PMID: 29089220 French.
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, Eliot MM, David A, Calais C, Drouin-Garraud V, Obstoy MF, Tran Ba Huy P, Lacombe D, Duriez F, Francannet C, Bitoun P, Petit C, Garabédian EN, Couderc R, Marlin S, Denoyelle F. Albert S, et al. Among authors: marlin s. Eur J Hum Genet. 2006 Jun;14(6):773-9. doi: 10.1038/sj.ejhg.5201611. Eur J Hum Genet. 2006. PMID: 16570074
[Genetic deafness in adults].
Marlin S, Jonard L, Feldmann D, Loundon N, Rouillon I, Couderc R, Denoyelle F. Marlin S, et al. Rev Prat. 2009 May 20;59(5):630-1. Rev Prat. 2009. PMID: 19552200 French. No abstract available.
Molecular diagnosis of genetic deafness.
Jonard L, Marlin S, Louha M, Bonnet C, Couderc R, Garabedian N, Denoyelle F; all the team of Centre de Référence des Surdités Génétiques, Hôpital Trousseau, APHP, Paris, France. Jonard L, et al. Among authors: marlin s. Clin Biochem. 2011 May;44(7):510-511. doi: 10.1016/j.clinbiochem.2011.02.031. Clin Biochem. 2011. PMID: 22036352 No abstract available.
[Genetic aspects of congenital sensorineural hearing loss].
Blanchard M, Thierry B, Marlin S, Denoyelle F. Blanchard M, et al. Among authors: marlin s. Arch Pediatr. 2012 Aug;19(8):886-9. doi: 10.1016/j.arcped.2012.05.015. Epub 2012 Jul 4. Arch Pediatr. 2012. PMID: 22770557 French.
SOX10 mutations mimic isolated hearing loss.
Pingault V, Faubert E, Baral V, Gherbi S, Loundon N, Couloigner V, Denoyelle F, Noël-Pétroff N, Ducou Le Pointe H, Elmaleh-Bergès M, Bondurand N, Marlin S. Pingault V, et al. Among authors: marlin s. Clin Genet. 2015 Oct;88(4):352-9. doi: 10.1111/cge.12506. Epub 2014 Nov 6. Clin Genet. 2015. PMID: 25256313
Unilateral Sensorineural Hearing Loss: Medical Context and Etiology.
Paul A, Marlin S, Parodi M, Rouillon I, Guerlain J, Pingault V, Couloigner V, Garabedian EN, Denoyelle F, Loundon N. Paul A, et al. Among authors: marlin s. Audiol Neurootol. 2017;22(2):83-88. doi: 10.1159/000474928. Epub 2017 Jul 22. Audiol Neurootol. 2017. PMID: 28738350
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: marlin s. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442
213 results