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

Molecular study and carrier detection of alpha thalassaemia in egypt

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

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

Study of VKORC1 polymorphism (C1173T) in Egyptian population

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

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

Study of factor V liden in thromboembolic patients

The co-existance of β-fibrinogen -455 G/A polymorphism and prothrombin 20210 G/A mutation in coronary heart disease in Egyptan patients