One of the most important literary forms in Persian poetry is Epic Romance. This romantic poems, from the point of view of the type of thought and subject, include the broadest part of …
Objective: Congenital hearing loss occurs in 1 out of 1000 births and about 50% of all cases are estimated to be of genetic origin. About 70% of hereditary hearing loss is non-syndromic …
Introduction: Hereditary Hearing loss (HHL) affects one in 2000 netborns and more than 50% of these cases, the loss has a genetic basis. About 70% of HHL is non-syndromic with …
Introduction: The serotonin transporter (5-HTT) gene is known as the responsible gene for interindividual variation and the genetic susceptibility for psychiatric diseases, such as bipolar …
Introduction: Hearing loss is the most common sensory neural defect in humans, affecting 1 in 1000 neonates, with over half of these cases predicted to be hereditary in nature. Most …
… Congenital blindness is frequently observed among a specific branch of the Lore tribe in the rural areas (Kheyr Abad) of the city of Sirjan in Kerman. This tribe is often alluded to as the …
Background: Dysfunction of the central dopaminergie neurotransmission has been suggested to play an important role in the etiology of SCHIZOPHRENIA. The dopamine transporter (…
tmuj.iautmu.ac.ir/article-1-4-en.htmlPDFBackground: Clonal gene rearrangement of immunoglobulin and T cell receptor may have mono, bi or oligoclonal pattern. Significance of these patterns were studied at diagnosis and …
In the diagnosis of PENDRED SYNDROME, assessment of individuals by molecular analysis of the SLC26A4 gene is recommended. Here we report a novel mutation in the SLC26A4 …
Introduction eta-thalassemia is the most common hereditary disease in Iran and more than 2 million carriers of the β-thalassemia mutant gene are living in this country. 1, 2 About 110 …