Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family von Wafa, Abdulsamad, Ali, Belal, Moassass, Faten, Kheder, Maged, Aljapawe, Abdulmunim, Al‐Halabi, Bassel, Mrasek, Kristin, Liehr, Thomas, Al‐Achkar, Walid

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Precancerous Lesions in Colorectal Cancer von Sandouk, Fayez, al-Jerf, Feras, al-Halabi, M. H. D. Bassel

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De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report von Alarbeed, Ismael F, Wafa, Abdulsamad, Moassass, Faten, Al-Halabi, Bassel, Al-Achkar, Walid, Liehr, Thomas, Aboukhamis, Imad

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The Clinical Impact of NPM1 Mutations and the Effect of Concurrent Mutations in Acute Myeloid Leukemia: Unraveling the Prognostic Significance von Moassass, Faten, Moualla, Yahia, AL‐Halabi, Bassel, Khamis, Atieh, Al‐achkar, Walid

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Investigation of some genetic variations in BMP15 accompanied with premature ovarian failure (POF) in Syrian women von Al-ajoury, Rana, Kassem, Essam, Al-halabi, Bassel, Moassess, Faten, Al-achkar, Walid

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Two Novel Mutations of the NPM1 Gene in Syrian Adult Patients with Acute Myeloid Leukemia and Normal Karyotype von Alarbeed, Ismael F., Wafa, Abdulsamad, Moassass, Faten, Al-Halabi, Balssel, Alachkar, Walid, Aboukhamis, Imad

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Evaluating the clinical significance of FLT3 mutation status in Syrian newly diagnosed acute myeloid leukemia patients with normal karyotype von Moualla, Yahia, Moassass, Faten, AL-Halabi, Bassel, Al-achkar, Walid, Georgeos, Michael, Yazigi, Haissam, Khamis, Atieh

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Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss von Moassass, Faten, Al-Halabi, Bassel, Nweder, Mohamad Sayah, Al-Achkar, Walid

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Mutations of the Connexin 26 gene in families with non-syndromic hearing loss von Al-Achkar, Walid, Moassass, Faten, Al-Halabi, Bassel, Al-Ablog, Ayman

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Prognostic Relevance of DNMT3A, FLT3 and NPM1 Mutations in Syrian Acute Myeloid Leukemia Patients von Moualla, Yahia, Moassass, Faten, AL-Halabi, Bassel, Al-Achkar, Walid, Georgeos, Michael, Yazigi, Haissam, Khamis, Atieh

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Frequency of FLT3 Internal Tandem Duplications in Adult Syrian Patients with Acute Myeloid Leukemia and Normal Karyotype von Al-Arbeed, Ismael F, Wafa, Abdulsamad, Moassass, Faten, AL-Halabi, Bassel, Al-Achkar, Walid, Abou-Khamis, Imad

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First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss von AL-Achkar, Walid, AL-Halabi, Bassel, Ali, Bashar, Moassass, Faten

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