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Hanen Belguith

Research Profile

Geographic Areas

Genes & Molecular Sequences

Recessive Genes

Disorders

Concepts & Ideas

Chemicals & Drugs

Anatomy

Physiology

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Publications

TOP 3
Olfa Siala; Ikhlass Hadj Salem; Abdelaziz Tlili; Imen Ammar; Hanen Belguith; Faiza Fakhfakh
Novel sequence variations in LAMA2 andSGCG genes modulating cis-acting regulatory elements and RNA secondary structure.
Lynn Adaimy; Eliane Chouery; Hala Megarbane; Salman Mroueh; Valérie Delague; Elsa Nicolas; Hanen Belguith; Philippe de Mazancourt; André Megarbane
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.
Hanen Belguith; S Hajji; N Salem; Ilhem Charfeddine; Imed Lahmar; M B Amor; Karim Ouldim; Eliane Chouery; Nabil Driss; Mohamed Drira; André Mégarbané; Ahmed Rebai; abdelaziz sefiani; Saber Masmoudi; Hammadi Ayadi
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.

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All Publications

2010: Olfa Siala; Ikhlass Hadj Salem; Abdelaziz Tlili; Imen Ammar; Hanen Belguith; Faiza Fakhfakh
Novel sequence variations in LAMA2 andSGCG genes modulating cis-acting regulatory elements and RNA secondary structure.
Genetics and molecular biology 2010;33(1):190-7.
2007: Lynn Adaimy; Eliane Chouery; Hala Megarbane; Salman Mroueh; Valérie Delague; Elsa Nicolas; Hanen Belguith; Philippe de Mazancourt; André Megarbane
Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia.
American journal of human genetics 2007;81(4):821-8.
2005: Hanen Belguith; S Hajji; N Salem; Ilhem Charfeddine; Imed Lahmar; M B Amor; Karim Ouldim; Eliane Chouery; Nabil Driss; Mohamed Drira; André Mégarbané; Ahmed Rebai; abdelaziz sefiani; Saber Masmoudi; Hammadi Ayadi
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.
Clinical genetics 2005;68(2):188-9.
2004: Saber Masmoudi; Ilhem Charfedine; I B Rebeh; Ahmed Rebai; Abdelaziz Tlili; Ali Ghorbel; Hanen Belguith; Christine Petit; Mohamed Drira; Hammadi Ayadi
Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Clinical genetics 2004;66(4):358-64.

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