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Author/Creator Ouederni, Monia

1. Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and Italy. (17th November 2019)

Authors:
Weslati, Ramla; Ouederni, Monia; Ruffo, Giovanbattista; Khaled, Monia Ben; Kouki, Ridha; Di Girgenti, Caterine; Borsellino, Zelia; Sammartano, Irene; El Gazzah, Mohamed; El- Bok, Safia; Bejaoui, Mohamed
Journal:
Annals of human biology
Issue:
Volume 46:Number 7/8(2019)
Page Start:
610
Record Type:
Journal Article
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3. High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis. Issue 2 (5th February 2014)

Authors:
Amouri, Ahlem; Talmoudi, Faten; Messaoud, Olfa; d'Enghien, Catherine D.; Rekaya, Mariem B.; Allegui, Ines; Azaiez, Héla; Kefi, Rym; Abdelhak, Ahlem; Meseddi, Sondes H.; Torjemane, Lamia; Ouederni, Monia; Mellouli, Fethi; Abid, Héla B.; Aissaoui, Lamia; Bejaoui, Mohamed; Othmen, Tarek B.; Lyonnet,...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 2:Issue 2(2014:Mar.)
Page Start:
160
Record Type:
Journal Article
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4. Long-Term Observational Study of Chronic Granulomatous Disease About 41 Patients From Tunisia and Comparison to Other Long-Term Follow-Up Studies. (October 2022)

Authors:
Mellouli, Fethi; Ksouri, Habib; Lajhouri, Maïssa; Ben Khaled, Monia; Rekaya, Samia; Ben Fraj, Elhem; Ouederni, Monia; Barbouche, Mohamed Ridha; Bejaoui, Mohamed
Journal:
Clinical pediatrics
Issue:
Volume 61:Number 9(2022)
Page Start:
629
Record Type:
Journal Article
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5. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)0-Thalassemia among Tunisian family. (March 2023)

Authors:
Kalai, Miniar; Moumni, Imen; Ouragini, Houyem; Ben Fraj, Ilhem; Mellouli, Fethi; Ouederni, Monia; Chaouachi, Dorra; Boudriga, Imen; Menif, Samia
Journal:
Annals of clinical biochemistry
Issue:
Volume 60:Number 2(2023)
Page Start:
81
Record Type:
Journal Article
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