Now showing items 1021-1024 of 1024
Novel missense mutation at codon 2774 (C.8321 G>A) p.S2774n of APC gene in a denovo case of familial adenomatous polyposis
Familial adenomatous polyposis (FAP) is an autosomal dominant inherited disease caused by germline mutation in Adenomatous Polyposis Coli (APC) gene. FAP accounts less than 1% of all colorectal cancers incidence. Patients ...
New insights into HLA class I association to Behط£آ§et's syndrome in Iranian Azari patients
Behط£آ§et's syndrome (BS) is a chronic recurrent inflammatory disorder characterized by oral and genital ulcers and ocular inflammation. BS has a complex genetic etiology. To evaluate the influence of human leukocyte antigen ...
Molecular Study of Deletional and Nondeletional Mutations on the ?-Globin Locus in the Azeri Population of Northwestern Iran
The aim of this study was to determine the molecular spectrum and frequency of deletional and nondeletional ?-thalassemia (?-thal) mutations and the genotype-phenotype correlation in common mutations in the Azeri population ...
Necessity of an integrated road traffic injuries surveillance system: A community-based study
Objectives: A prerequisite to improving the situation of traffic accidents and injury prevention is to set up a road traffic accident and victim information system (RTAVIS), which does not exist in Iran. The objective of ...