Mutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia

Thrombophilic gene mutations in cases with recurrent miscarriage : A study in the Egyptian Population

The effect of methylenetetrahydrofolate reductase gene mutation on plasma homocysteine and incidence in arterial diseases

Study of methylenetetraydrofolate reductase gene mutation as a risk factor for deep venous thrombosis

Study of VKORC1 polymorphism (C1173T) in Egyptian population

Identification of common mutationscausing Wilson disease in Egyptian children

Molecular diagnosis of mitochondrial and nuclear DNA mutations among Egyptian children with mitochondrial encephalomyopathies

Maternal and off-spring methylenetetrahydrofolatereductase Gene C677T polymorphism;does it influence the prevalence of congenitalheart defects in Eyptian neonates?

Molecular characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children

Genetic study in Egyptian children with Wilson disease