Molecular study of factor VIII gene in Egyptian patients with hemophilia A

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

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

Identification of common mutationscausing Wilson disease in Egyptian children

Identification of some genetic markers in familial breast cancer in Egyptian patients

Molecular study and carrier detection of alpha thalassaemia in egypt

Genetic susceptibility to psoriasis: A genome wide association study in Egyptian psoriatic patients

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

Detection of CXCl12 gene polymorphism and CXCR 4 receptor expression in Egyptian acute myeloid leukemia patients

Molecular detection of intron 22 inversion of factor VIII gene in Egyptian hemophilia A patients