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Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low‐GGT intrahepatic cholestasis: Genetic diagnosis and genot... von Khabou, Boudour, Kallabi, Fakhri, Abdelaziz, Rim Ben, Maaloul, Ines, Aloulou, Hajer, Chehida, Amel ben, Kammoun, Thouraya, Barbu, Veronique, Boudawara, Tahya Sellami, Fakhfakh, Faiza, Khemakhem, Bassem, Sahnoun, Olfa Siala

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Genetic analysis of Turner syndrome in Tunisian patients: from diagnosis to management von Siala-Sahnoun, Olfa, Laadhar, Fatma, Mnif, Mouna, Sefi, Wajdi, Kacem, Faten, Kessentini, Mohamed, Abid, Mohamed, Fakhfakh, Faiza

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In silico investigation of the impact of synonymous variants in ABCB4 gene on mRNA stability/structure, splicing accuracy and codon usage: Potential contribution to PFIC3 disease von Khabou, Boudour, Siala-Sahnoun, Olfa, Gargouri, Lamia, Mkaouar-Rebai, Emna, Keskes, Leila, Hachicha, Mongia, Fakhfakh, Faiza

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First molecular diagnosis of Donohue syndrome in Africa: novel unusual insertion/deletion mutation in the INSR gene von Siala-Sahnoun, Olfa, Dhieb, Dhoha, Ben Thabet, Afef, Hmida, Nedia, Belguith, Neila, Fakhfakh, Faiza

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