Alteration of B and T cell markers in chronic granulomatous disease (CGD) patients

Detection of RAG1 and RAG2 mutations in patients diagnosed as severe combined immunodeficiency/ combined immunodeficiency

The use of dihydrorhodamine for flowcytometric analysis of the neutrophil respiratory burst in suspected cases of chronic granulomatous disease

Detection of glutathione-stransferasenull genotypes in acute and chronic myeloid leukaemias

Genotype phenotype relationship in gaucher's disease

Myeloperoxidase in serum of cancer patients under treatment and their susceptibility to candida infection

Genotype and phenotype correlation in glucose-6- phosphate dehydrogenase deficiency

Study of mutation in NAD (P) H : Quinone oxidoreductase 1 alleles in patients with acute leukemia

Functional disorders of neutrophils

The role of fanconi anaemia genes in DNA repai