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Houria Dhouib

Showing results (1-10 of 7) with videos related to

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International Journal of Pediatric Otorhinolaryngology|March 21, 2012
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndromeMariem Ben Said, Houria Dhouib, Zeineb BenZina, et al.
La Tunisie Medicale|November 26, 2009
[Polymorphous low-grade adenocarcinoma: about two cases]Lobna Ayadi, Salma Chaâbouni, Houria Dhouib, et al.
Biochemical and Biophysical Research Communications|March 4, 2009
Mutation in gap and tight junctions in patients with non-syndromic hearing lossHanen Belguith, Abedelaziz Tlili, Houria Dhouib, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian familyMounira Hmani-Aifa, Zeineb Benzina, Fareeha Zulfiqar, et al.
Genetic Testing and Molecular Biomarkers|March 25, 2009
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locusHanen Belguith, Mounira Aifa-Hmani, Houria Dhouib, et al.
Audiology & Neuro-Otology|February 9, 2008
TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian familiesAbdelaziz Tlili, Imen Ben Rebeh, Mounira Aifa-Hmani, et al.
Molecular Vision|September 23, 2008
Identification of candidate regions for a novel Usher syndrome type II locusImen Ben Rebeh, Zeineb Benzina, Houria Dhouib, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
International Journal of Pediatric Otorhinolaryngology|March 21, 2012
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndromeMariem Ben Said, Houria Dhouib, Zeineb BenZina, et al.
La Tunisie Medicale|November 26, 2009
[Polymorphous low-grade adenocarcinoma: about two cases]Lobna Ayadi, Salma Chaâbouni, Houria Dhouib, et al.
Biochemical and Biophysical Research Communications|March 4, 2009
Mutation in gap and tight junctions in patients with non-syndromic hearing lossHanen Belguith, Abedelaziz Tlili, Houria Dhouib, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian familyMounira Hmani-Aifa, Zeineb Benzina, Fareeha Zulfiqar, et al.
Genetic Testing and Molecular Biomarkers|March 25, 2009
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locusHanen Belguith, Mounira Aifa-Hmani, Houria Dhouib, et al.
Audiology & Neuro-Otology|February 9, 2008
TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian familiesAbdelaziz Tlili, Imen Ben Rebeh, Mounira Aifa-Hmani, et al.
Molecular Vision|September 23, 2008
Identification of candidate regions for a novel Usher syndrome type II locusImen Ben Rebeh, Zeineb Benzina, Houria Dhouib, et al.
Pageof 1