Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification

A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus

Biochemical diagnosis of Wolman disease among patients with suspected lysosomal storage diseases

Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease

A rare mutation in an Egyptian family with Sanfilippo B syndrome

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

Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion

Cytogenetic study of a large cohort of patients with corpus callosum abnormalities

Bone-specific therapeutic modalities for genetic skeletal diseases

A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa

Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity

A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management