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Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis
Houyem Ouragini
,
Faïka Cherif
,
Wafa Daoud
,
Selma Kassar
,
Chérine Charfeddine
,
et al.
Journal articles
istex
pasteur-01375212v1
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Genetic analysis of hereditary multiple exostoses in Tunisian families: a novel frame-shift mutation in the EXT1 gene
Sana Sfar
,
Abderrazak Abid
,
Wijden Mahfoudh
,
Houyem Ouragini
,
Farah Ouechtati
,
et al.
Journal articles
istex
pasteur-01375178v1
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Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family
Houyem Ouragini
,
Faika Cherif
,
Selma Kassar
,
Giovanna Floriddia
,
Monica Pascucci
,
et al.
Journal articles
pasteur-01375196v1
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Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene.
Farah Ouechtati
,
Ahlem Merdassi
,
Yosra Bouyacoub
,
Leila Largueche
,
Kaouther Derouiche
,
et al.
Journal articles
pasteur-00604858v1
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Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families.
Sonia Nouira
,
Fatma Ouarda
,
Cherine Charfeddine
,
Imen Arfa
,
Houyem Ouragini
,
et al.
Journal articles
istex
pasteur-00612166v1
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Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis
Houyem Ouragini
,
Fayrouz. Haddad
,
Imen Darragi
,
Salem Abbes
Journal articles
pasteur-01375110v1
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Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.
Ahlem Sabrine Ben Brick
,
Nadia Laroussi
,
Hela Mesrati
,
Rym Kefi
,
Mbarka Bchetnia
,
et al.
Journal articles
pasteur-01061249v1
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Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia
Nizar Ben Halim
,
Sana Hsouna
,
Khaled Lasram
,
Insaf Rejeb
,
Asma Walha
,
et al.
Journal articles
pasteur-01374977v1
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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients
Leila Chaouch
,
Imen Moumni
,
Houyem Ouragini
,
Imen Darragi
,
Miniar Kalai
,
et al.
Journal articles
pasteur-01374983v1
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Clinical and Genetic Investigation of Atrial Septal Defect with Atrioventricular Conduction Defect in a Large Consanguineous Tunisian Family
Sonia Nouira
,
Ikram Kamoun
,
Houyem Ouragini
,
Cherine Charfeddine
,
Haifa Mahjoub
,
et al.
Journal articles
pasteur-01375202v1
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The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients
Miniar Kalai
,
Marwa Dridi
,
Leila Chaouch
,
Imen Moumni
,
Houyem Ouragini
,
et al.
Journal articles
hal-01513653v1
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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
Zied Riahi
,
Hassen Hammami
,
Houyem Ouragini
,
Habib Messai
,
Rim Zainine
,
et al.
Journal articles
pasteur-00861409v1
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