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

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

Evaluation of the screening value of the activity of Chitotriosidase enzyme in plasma and in dried blood spots for the detection of lysosomal storage disorders

Mannose binding lectin (MBL2) gene variants in sickle cell disease

Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia

Study of some genetic ameliorating factors in homozygous beta thalassemia intermedia

Study of glutathione S-transferase gene polymorphisms in sickle cell anemia patients

Impact of prothrombotic risk factors on the clinical phenotype in haemophilia patients

Association of Factor XII genotypic polymorphism and phenotype with risk of venous thrombosis

Polymorphism of genes involved in susceptibility to acute lymphoblastic leukemia