DETECTION OF JAK2 MUTATION IN CASES OF MYELODYSPLASTIC SYNDROME

Expression of JAK2 V617F mutation in chronic myeloproliferative disorders

DETECTION OF CALR EXON 9MUTATIONS IN EGYPTIAN PATIENTS WITH PERSISTENT THROMBOCYTOSIS

DIAGNOSTIC VALUE OF JAK2 V617F MUTATIONAL SCREENING IN PATIENTS WITH BUDD-CHIARI SYNDROME

Detection of C-kit gene Mutation in Patients with Acute Myeloid Leukemia

Impact of JAK2V617F Mutational on Haematologic Features in Sudanese Patients with Essential Thrombocythemia and Thrombotic Risk Assessment

Detection of a Point Mutation at Codon 12 of the Kirsten-Ras (K-ras) Oncogen in Myelodysplastic Syndrome

Study and Survey of BCR-ABL Transcript Types in Chronic Myeloid Leukemia (CML) Young Egyptian Patients

Significance of CAL2 by Immunohistochemistry in Detecting CALR Mutation in Egyptian Patients with BCR- ABL Negative Myeloproliferative Neoplasms

Evaluating The Risk of Thrombosis and Its Relation to JAKII Mutation in Egyptian Myeloproliferative Neoplasm Patients