Study of the association of protein tyrosine phosphatase non receptor Type 22 (PTPN22) C1858T gene polymorphism with type 1 diabetes mellitus

Genetics of type 1 diabetes mellitus in Egyptian patients

Thyroid autoimmunity in Egyptian children with insulin-dependent (type 1) diabetes mellitus : Pilot study

DNMT3B 579G>T promoter polymorphism and the risk for idiopathic thrombocytopenic purpura : An Egyptian study

Association between interleukin 17A and interleukin 17F gene polymorphisms and the susceptibility to acute myeloid leukemia in adult Egyptians

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

Mutation analysis of steroid 21 hydroxylase gene in a group of Egyptian children with congenital adrenal hyperplasia

Study of T-cell immunoglobulin- and mucin-domain-containing molecule 3 polymorphisms in Egyptian patients with idiopathic thrombocytopenic purpura

Genetic variation in Interleukin-2 and Interleukin-10 and the susceptibility to B-cell Non-Hodgkin Lymphoma in a group of Egyptian patients

The association between KIR 6.2 mutations and type 1 diabetes