ThesisMolecular characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children
ThesisMolecular characterization of 21 hydroxylase deficiency of congenital adrenal hyperplasia in Egyptian children
ThesisMutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia
ThesisMutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia
ThesisGenetic susceptibility to psoriasis: A genome wide association study in Egyptian psoriatic patients
ThesisGenetic susceptibility to psoriasis: A genome wide association study in Egyptian psoriatic patients
ThesisMolecular diagnosis of mitochondrial and nuclear DNA mutations among Egyptian children with mitochondrial encephalomyopathies
ThesisMolecular diagnosis of mitochondrial and nuclear DNA mutations among Egyptian children with mitochondrial encephalomyopathies
ThesisDetection of CXCl12 gene polymorphism and CXCR 4 receptor expression in Egyptian acute myeloid leukemia patients
ThesisDetection of CXCl12 gene polymorphism and CXCR 4 receptor expression in Egyptian acute myeloid leukemia patients
ThesisMolecular detection of intron 22 inversion of factor VIII gene in Egyptian hemophilia A patients
ThesisMolecular detection of intron 22 inversion of factor VIII gene in Egyptian hemophilia A patients