Network Profiles
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Twitter Profile: Saber Masmoudi (saber70)
Location: Tunis - TUNISIA / Engineer; A news addicted; Against censorship; For freedom.
ICQ User saber Masmoudi (sabi)
, Male, Age: 33, Recklinghausen, Country: Germany, German, English, Arabic
Interests
Determination of the frequency of connexin26 mutations in inherited...
jmg.bmj.com
saber masmoudi *, amel elgaied-boulila *, ilyes kassab †, saida ben arab * ...
Business Profiles
Xing: Saber Masmoudi
Berater / Recklinghausen / Erfahrungen im bereich:
- Finanzmanagement
- Marketing im bereich logistik und Einkauf
- Fachberater im Versicherungswesen
- Kaufmann in Handel u. Industrie
- Prokurist / Union Investment, Mira Maxdata AG
Researchgate: Saber Masmoudi
Sfax, Tunisia
Private Homepages
Editorial Team - Ivy Union Publishingivyunion.org/index.php/genetics/about/editorialTeamBio/2251
ivyunion.org
... Nadia Mahfoudh, Adnene Ayadi, Abdullah Gibriel, Bakhta Mallek, Leila Maalej, Zouheir Hammami, Samir Maatoug, Hafedh Makni, Saber Masmoudi
Books & Literature
Molecular Vision: Articles by the Authors
www.molvis.org
Articles by Imen Hadjamor · Articles by Hammadi Ayadi · Articles by Abdelmonem Ghorbel · Articles by Christine Petit · Articles by Saber Masmoudi.
Related Documents
CiteSeerX — that associates with
citeseerx.ist.psu.edu
@MISC{Weil02thatassociates, author = {Dominique Weil and Aziz El-amraoui and Saber Masmoudi and Mirna Mustapha and Yoshiaki Kikkawa and Sedigheh Delmaghani and …
A mutation in SLC22A4 encoding an organic cation transporter...
www.deepdyve.com
Mariem Ben Said and M'hamed Grati have contributed equally. to this work. * Saber Masmoudi. .tn. * Xuezhong Liu.
Whole mitochondrial genome screening in two families with hearing...
portlandpress.com
Emna Mkaouar-Rebai, Nourhene Fendri-Kriaa, Nacim Louhichi, Abdelaziz Tlili, Chahnez Triki, Abdelmoneem Ghorbel, Saber Masmoudi, Faiza ...
Mutations of LRTOMT, a fusion gene with alternative reading frames,...
www.scienceopen.com
Authors: Zubair M Ahmed, Saber Masmoudi, Ersan Kalay,,, Inna A Belyantseva, Mohamed Ali Mosrati, Rob W J Collin,, Saima Riazuddin, ...
Scientific Publications
A missense mutation in DCDC2 causes human recessive deafness DFNB66,...
www.ncbi.nlm.nih.gov
... with sensory hair cell and supporting cell cilia length regulation. M'hamed Grati, Imen Chakchouk, [...], and Saber Masmoudi. Additional article information ...
Annual Acknowledgement of Reviewers | BMC Medical Genomics | Full Text
bmcmedgenomics.biomedcentral.com
Annual Acknowledgement of Reviewers The editors of BMC Medical Genomics would like to thank all our reviewers who have contributed to the ... Saber Masmoudi ...
Publications
High Frequency of the p.R34X Mutation in the TMC1 Gene Associated...
core.ac.uk
... Delmaghani, Abdelaziz Tlili, Abdelmonem Ghorbel, Hammadi Ayadi, Guy Van Camp, Richard J. H. Smith, Mustafa Tekin and Saber Masmoudi ...
A mutation in SLC22A4 encoding an organic cation transporter...
link.springer.com
Saber Masmoudi (1) Zhongmin Lu (4) Mounira Hmani (1) Xuezhong Liu (2) (7) (8) Author Affiliations. 1. Laboratoire Procédés de Criblage Moléculaire et Cellulaire ...
Oalib search
www.oalib.com
Ibtihel Smeti, Said Assou, Etienne Savary, Saber Masmoudi, Azel Zine PLOS ONE , 2012, DOI: journal.pone Abstract ...
Video & Audio
Saber Masmoudi - YouTube
www.youtube.com
Teile deine Videos mit Freunden, Verwandten oder der ganzen Welt
Reports & Statements
Genome-wide analysis reveals a novel autosomal-recessive hearing loss...
www.nature.com
Original Article
Articles in | Journal of Human Genetics
www.nature.com
Browse the archive of articles on Journal of Human Genetics
Miscellaneous
Saber Masmoudi | LinkedIn
www.linkedin.com
View Saber Masmoudi's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Saber Masmoudi discover inside ...
Saber Masmoudi | Sfax University Tunisia - Academia.edu
uss-tn.academia.edu
Academia.edu is a place to share and follow research.
Discovery of Critical Gene Mutation Linked to Hereditary Deafness...
www.audiologyonline.com
A gene mutation causing a form of hereditary deafness has been identified by an international team of researchers led by Xuezhong Liu, M.D., Ph.D., at the...
Amissense mutation in DCDC2 causeshuman recessive deafness DFNB66,...
miami.pure.elsevier.com
... Nouha Turki, Denise Yan, Aissette Baanannou, Rahul Mittal, Nabil Driss, Susan H Blanton, Amjad Farooq, Zhongmin Lu, Xue Z Liu, Saber Masmoudi.
Journal of Audiology & Otology
www.ejao.org
... Mohamed Noureddine Alami, Abdelaziz Tlili, Hassan Rouba, Saber Masmoudi, Abdelaziz Chafik, Mohammed Hassar, Abdelhamid Barakat.
(PDF) Identification of candidate regions for a novel Usher syndrome...
www.academia.edu
Identification of candidate regions for a novel Usher syndrome type II locus Dr. Saber Masmoudi, Unité Cibles pour le Diagnostic et la Thérapie, ...
FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum...
en.x-mol.com
X-MOL提供的期刊论文更新，American Journal of Human Genetics——FDXR Mutations Cause Sensorial Neuropathies and Expand the Spectrum of Mitochondrial Fe-S-Synthesis...
Sfax University Tunisia | Center of Biotechnology of Sfax-Tunisia -...
uss-tn.academia.edu
The Center of Biotechnology of Sfax-Tunisia at Sfax University Tunisia on Academia.edu
Hearing Loss CDWG - ClinGen | Clinical Genome Resource
www.clinicalgenome.org
The Hearing Loss Working Group aims to create a comprehensive, standardized knowledge base of genes and variants relevant to syndromic and nonsyndromic hearing...
Identification of Genes Causing Syndromic And Nonsyndromic Hearing...
grantome.com
The goal of the Section on Human Genetics is to identify genes for Usher syndrome and nonsyndromic forms of hereditary deafness. This work begins with the...
Altmetric – Spectrum of DNA variants for non-syndromic deafness in a...
www.altmetric.com
... Claudia Carranza, Reza Maroofian, Andrew H. Crosby, Mariem Bensaid, Saber Masmoudi, Mahdiyeh Behnam, Majid Mojarrad, Yong Feng, ...
Mutations in a new gene encoding a protein of the hair bundle cause...
go.gale.com
Author(s): Elisabeth Verpy [1]; Saber Masmoudi [1, 2]; Ingrid Zwaenepoel [1]; Michel Leibovici [1]; Tim P. Hutchin [3]; Ignacio Del Castillo [4]; Sylvie Nouaille [1]; ...
(PDF) Two missense mutations in SLC26A4 gene: a molecular and...
www.academia.edu
By Saber Masmoudi in Genetics and Family a molecular and functional study Ben Rebeh I, ... Two missense mutations in SLC26A4 gene: ...
Molecular Analysis of Libyan Families with Allgrove Syndrome:...
read.qxmd.com
Fakhri Kallabi, Imen Ben Rebeh, Rahma Felhi, Dorra Sellami, Saber Masmoudi, Leila Keskes, Hassen Kamoun. Hormone Research in Pædiatrics 2016, 85 (1): ...
Résultat de la présélection des dossiers de candidature MOBIDOC-...
docplayer.fr
... Biotechnologie de Sfax (CBS) Saber Masmoudi 104 Safia MESSAOUDI Laboratoire de génome humain et des maladies Touhami MAHJOUB multifactorielles, ...
Usher syndrome type I G (USH1G) is caused by mutations in the gene...
paperity.org
Paperity: the 1st multidisciplinary aggregator of Open Access journals & papers. Free fulltext PDF articles from hundreds of disciplines, all in one place
Internet Scientific Publications
ispub.com
Hammadi Ayadi Unité Cibles pour le Diagnostic et la Thérapie, Centre de Biotechnologie de Sfax, Tunisie. Saber Masmoudi Unité Cibles pour le Diagnostic et ...
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