Clinical and Genetic Study of Exons (23, 24, 26, 27) of ABCB11 Gene in Egyptian Progressive Familial Intrahepatic Cholestasis 2 Patients

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

Molecular Diagnosis of Hepatocellular Carcinoma in Egypt

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

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

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

The Correlation between Single Nucleotide Polymorphism of MBOAT7 and PNPLA3 Genes to The Degree of Hepatic Fibrosis in HCV Patients: An Experience from Egypt

The Influence of C936T Gene Polymorphism of the vascular endothelial growth factor and biochemical variants for Alpha-Fetoprotein in hepatocellular carcinoma Patients in Egypt

MOLECULAR BASIS OF BETA THALASSEMIA MUTATIONS IN EGYPTIAN PATIENTS