Ben Arab S - Search Results

1

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C. Guilford P, et al. Among authors: ben arab s. Nat Genet. 1994 Jan;6(1):24-8. doi: 10.1038/ng0194-24. Nat Genet. 1994. PMID: 8136828

2

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. Hum Mol Genet. 1997 Nov;6(12):2173-7. doi: 10.1093/hmg/6.12.2173. Hum Mol Genet. 1997. PMID: 9336442

3

An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul).

Ben Arab S, Bonaïti-Pellié C, Belkahia A. Ben Arab S, et al. J Med Genet. 1990 Jan;27(1):29-33. doi: 10.1136/jmg.27.1.29. J Med Genet. 1990. PMID: 2308153 Free PMC article.

4

Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates.

Ben Arab S, Hmani M, Denoyelle F, Boulila-Elgaied A, Chardenoux S, Hachicha S, Petit C, Ayadi H. Ben Arab S, et al. Clin Genet. 2000 Jun;57(6):439-43. doi: 10.1034/j.1399-0004.2000.570607.x. Clin Genet. 2000. PMID: 10905664

5

A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9.

Bel Hadj Ali I, Thys M, Beltaief N, Schrauwen I, Hilgert N, Vanderstraeten K, Dieltjens N, Mnif E, Hachicha S, Besbes G, Ben Arab S, Van Camp G. Bel Hadj Ali I, et al. Among authors: ben arab s. Hum Genet. 2008 Apr;123(3):267-72. doi: 10.1007/s00439-008-0470-3. Epub 2008 Jan 26. Hum Genet. 2008. PMID: 18224337 Clinical Trial.

6

[Epidemiological study of otospongiosis in the Nabeul region].

Ben Arab S, Marrakchi A, Belkahia A. Ben Arab S, et al. Tunis Med. 1994 Jan;72(1):19-24. Tunis Med. 1994. PMID: 8203025 French. No abstract available.

7

A genetic study of otosclerosis in a population living in the north of Tunisia.

Ben Arab S, Bonaïti-Pellié C, Belkahia A. Ben Arab S, et al. Ann Genet. 1993;36(2):111-6. Ann Genet. 1993. PMID: 8215216

8

Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE.

Masmoudi S, Elgaied-Boulila A, Kassab I, Ben Arab S, Blanchard S, Bouzouita JE, Drira M, Kassab A, Hachicha S, Petit C, Ayadi H. Masmoudi S, et al. Among authors: ben arab s. J Med Genet. 2000 Nov;37(11):E39. doi: 10.1136/jmg.37.11.e39. J Med Genet. 2000. PMID: 11073548 Free PMC article. No abstract available.

9

Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness.

Ben Arab S, Masmoudi S, Beltaief N, Hachicha S, Ayadi H. Ben Arab S, et al. Genet Epidemiol. 2004 Jul;27(1):74-9. doi: 10.1002/gepi.10321. Genet Epidemiol. 2004. PMID: 15185405

10

Genetic heterogeneity study of non-syndromic autosomal recessive sensorineural deafness within the Tunisian population.

Chaabani H, Ben Arab S, Chebbi K. Chaabani H, et al. Among authors: ben arab s. Ann Genet. 1995;38(3):158-61. Ann Genet. 1995. PMID: 8540687

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