Assessment of serum level of vitamin D in infants and children with Down syndrome

Dysregulation of tumor necrosis factor-α and interleukin-6 as predictors of gestational disorders

Genetic study of the association of specific language impairment to markers near gene

MicroRNA-mediated sensitization of lung cancer cells to chemotherapeutics: the roles of miR-21 and miR-155

Fragile X syndrome: diagnosis by molecular characterization of gene and clinical correlation

Clinical and cytogenetic analysis of terminal 22q13.3 deletion in two patients with ring chromosome 22

Updates about ethical, legal and psychological implications of genetic testing in newborns, children and adolescents

Genetic syndromes with immunological disturbances

Genome-editing technologies: Advancement, clinical applications, and ethical concerns

Corpus callosum abnormalities in 64 Egyptian patients: Neuropsychological and genetic studies

Mutation analysis of the arylsulfatase B gene among Egyptian patients with Maroteaux–Lamy disorder