Alpha-thalassemia (α-thal) is probably the most prevalent monogenic condition in the world. Deletions are the most common types of mutations in α-thal, followed by point mutations and small insertion/deletion. In the context of national screening program for prevention of thalassemia and hemoglobinopathies in Iran, α-thal carriers have come to more attention. Therefore, the frequency and distri...

a total of 8641 married couples were investigated from 28 iranian populations for consanguineous marriages and coefficient of inbreeding. the results showed considerable differences in the rate and kind of consanguineous matings among the various urban, rural, tribal, and religious populations studied. the observed frequencies of the consanguineous matings in the populations of iran are higher ...

Mutations in the Connexin 26 (Cx26) gene are a common cause of hereditary hearing loss in different populations. In the present study, an Iranian patient with bilateral hearing loss underwent molecular analysis for the causative mutation. DNA studies were performed for the Cx26 gene by PCR and sequencing methods. We describe a novel compound heterozygous mutation (35delG, 363delC) in the Cx26 g...

Maxillary lateral incisors are widely known to be single rooted with one root canal. Although rare cases with root canal variations are being reported in many populations, the reports regarding Iranian population is extremely limited. In this report, we are presenting the endodontic treatment of a double rooted maxillary lateral incisor. These rare root-canal variations should be considered in ...

inter simple sequence repeat (issr) markers were used to assess the genetic diversity among 23 outcross and self pollinated populations of fennel collected from different geographical regions of iran and some european countries. the experiment was carried out to determine the effect of self-pollination on morphological traits and genetic diversity in the next generation. fifteen primers produce...

Bovine spongiform encephalopathy (BSE) is a fatal infectious neurodegenerative disease in cattle, characterized by the accumulation of an abnormal, proteaseresistant prion protein (PrPSc) in the brain. BSE is similar to scrapie in sheep and goats and Creuzfeldt-Jakob disease in humans. Susceptibility in cattle hasbeen shown to be under the influence of two polymorphic locations, which are...