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

Prevalence of –alpha 3.7 and alpha4.2 alpha thalassaemia deletions among Egyptians using cord blood

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

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

Genetic screening for alpha thalassemia mutations among Egyptian neonates

Identification of common mutationscausing Wilson disease in Egyptian children

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

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

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

Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia