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

Clinical biochemical markers for hepatocellular carcinoma in Egyptian patients

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

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

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

Molecular study and carrier detection of alpha thalassaemia in egypt

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

The prevalence of p53 gene mutation in hepatocellular carcinoma in Egyptians

Some potential genetic markers for prediction of treatment response in HCV affected Egyptian children