Clinical and Molecular Study of Exons [10-14] of ABCB11 Gene in PFIC2 Patients in Egypt

Phenotypic Study of Egyptian Pediatric Patients with Criglar Najjar Syndrome

ABCB11 gene mutations in children with progressive familial intrahepatic cholestasis (PFIC) and low GGT

Association of PNPLA3 Gene Polymorphisms with the Development and Progression of Hepatocellular Carcinoma in Egyptian patients"

Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study

A Genetic Risk Factor in Egyptian Children with A Family History of End-Stage Renal Disease

Clinical and Molecular Characterization of Achondroplasia in Egyptian Patients

Detection of SMARCB1 gene mutations in Egyptian hepatocellular carcinoma patients using targeted next-generation sequencing: A pilot study

A Study of Hepcidin Gene Polymorphism in Beta Thalassemia Major Egyptian Patients Refractory to Iron Chelation

TM6SF2 RS58542926 IS LINKED TO THROMBOCYTOPENIA-RELATED ADVANCED HEPATIC FIBROSIS IN EGYPTIAN PATIENTS WITH CHRONIC HEPATITIS C