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

Detection of sites of pointmutations in some exons of thefactor VIII gene in hemophilia Apatients

Molecular study and carrier detection of alpha thalassaemia in egypt

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

Study of VKORC1 polymorphism (C1173T) in Egyptian population

Identification of some genetic markers in familial breast cancer in Egyptian 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 characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children

Study of the coagulation factor VII gene polymorphism in patients undergoing coronary catheter intervention