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

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

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

Characterization of 42 Egyptian Children with Lysosomal Storage Disorders

Descriptive Study of the Different Phenotypes of Congenital Heart Disease in a Cohort of Egyptian Patients Diagnosed with Down Syndrome

SCREENING OF EGYPTIAN PATEINTS SUFFERING FROM INBORN AMINO ACID METABOLIC DISORDERS

A rare mutation in an Egyptian family with Sanfilippo B syndrome

Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients

Patterns of idiopathic nephrotic syndrome in Upper Egyptian children

Clinical phenotypes of renal cystic diseases in Egyptian children