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Marwa Haddaji Mastouri
Marwa Haddaji Mastouri
Genetics
Gene
Medicine
Exon
Missense mutation
4
Papers
23
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Genetic study of non‐syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case‐series
2018
European Journal of Oral Sciences
Marwa Haddaji Mastouri
Peter De Coster
Aicha Zaghabani
Frej Jammali
Nabiha Raouahi
Amina Ben Salem
Ali Saad
Paul Coucke
Dorra Hmida Ben Brahim
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Citations (5)
Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis
2016
Archives of Oral Biology
Marwa Haddaji Mastouri
Peter De Coster
Aicha Zaghabani
Saoussen Trabelsi
Yosra May
Ali Saad
Paul Coucke
Dorra Hmida Ben Brahim
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Citations (9)
Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor.
2015
Applied and Translational Genomics
Dorra Hmida Ben Brahim
Sabeur Hammami
Marwa Haddaji Mastouri
Saoussen Trabelsi
Maroua Chourabi
Sihem Sassi
Soumaya Mougou
Moez Gribaa
Abdelfattah Zakhama
Mohamed Neji-Guédiche
Ali Saad
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Citations (6)
Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes
2014
Genetics research international
Dorra Hmida Ben Brahim
Marwa Chourabi
Sana Ben Amor
Imed Harrabi
Saoussen Trabelsi
Marwa Haddaji Mastouri
Moez Gribaa
Sihem Sassi
Fatma Ezzahra Gahbiche
Turkia Lamouchi
Soumaya Mougou-Zereli
Sofiane Ben Ammou
Ali Saad
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Citations (3)
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