The prevalence of p53 gene mutation in hepatocellular carcinoma in Egyptians

P 53 mutations in tissue and blood in egyptian patientswith colorectal carcinoma and premalignant colonic lesions

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

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

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

Overexpression of her-2 neu in papillary thyroid carcinoma : Histopathological and immunohistochemical study

Cervical intraepithelial neoplasia in Egyptian patients : A histopathological and statistical study

Identification of common mutationscausing Wilson disease in Egyptian children

Vascular endothelial growth factor 634G/C gene polymorphism in prognosis of hepatocellular carcinoma in Egyptian patients