Ben Arab S - Search Results

1

Consanguinity, endogamy, and genetic disorders in Tunisia.

Ben Halim N, Ben Alaya Bouafif N, Romdhane L, Kefi Ben Atig R, Chouchane I, Bouyacoub Y, Arfa I, Cherif W, Nouira S, Talmoudi F, Lasram K, Hsouna S, Ghazouani W, Azaiez H, El Matri L, Abid A, Tebib N, Ben Dridi MF, Kachboura S, Amouri A, Mokni M, Ben Arab S, Dellagi K, Abdelhak S. Ben Halim N, et al. Among authors: ben arab s. J Community Genet. 2013 Apr;4(2):273-84. doi: 10.1007/s12687-012-0128-7. Epub 2012 Dec 4. J Community Genet. 2013. PMID: 23208456 Free PMC article. No abstract available.

2

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.

3

No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree.

Bougacha-Elleuch N, Ben Arab S, Rebai A, Mnif M, Maalej A, Charfi N, Ben Lassouad M, Jouida J, Abid M, Ayadi H. Bougacha-Elleuch N, et al. Among authors: ben arab s. J Genet. 2011 Aug;90(2):333-7. doi: 10.1007/s12041-011-0064-z. J Genet. 2011. PMID: 21869485 No abstract available.

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

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

7

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

8

[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.

9

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

10

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

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