Radwa Gamal

Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I

Genotype-phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants.

Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases

Meier-Gorlin syndrome: Report of an additional patient with congenital heart disease

Bilateral iris, choroid, optic nerve colobomas and retinal detachment in an Egyptian patient with mild Baraitser–Winter syndrome

Removal notice to “An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings” [Egypt J Med Hum Genet 18 (2017) 393–396]

Cardiomyopathy in Vici syndrome

Cantu syndrome in an Egyptian child

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II

Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child