Molecular study and carrier detection of alpha thalassaemia in egypt

Genetic screening for alpha thalassemia mutations among Egyptian neonates

RBC alloimmunization in Egyptian blood transfusion dependent beta-thalassemia patients

Study of RH blood group alloimmunization in Egyptian neonates who suffer from hemolytic disease of the newborn

Identification of common mutationscausing Wilson disease in Egyptian children

DNA sequencing of uncharacterized β–globin gene mutations in β–thalassaemia in children

DNA sequencing of uncharacterized beta–globin gene mutations in beta–thalassaemia in children

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

G6PD gene polymorphisms in Egyptian deficient patients

The prevalence of human platelet antigen (HPA) 1a and 1bb groups among Egyptianpregnant females and the incidence of HPA1aalloimmunization in neonates