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Author:(Nasrin YAZDANPANAHI)

1.Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome.

Nasrin YAZDANPANAHI ; Mohammad Amin TABATABAIEFAR ; Effat FARROKHI ; Narges ABDIAN ; Nader BAGHERI ; Shirin SHAHBAZI ; Zahra NOORMOHAMMADI ; Morteza Hashemzadeh CHALESHTORI

Clinical and Experimental Otorhinolaryngology 2013;6(4):201-208

2.Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran

Fatemeh AZADEGAN-DEHKORDI ; Tayyebe BAHRAMI ; Maryam SHIRZAD ; Gelareh KARBASI ; Nasrin YAZDANPANAHI ; Effat FARROKHI ; Mahbobeh KOOHIYAN ; Mohammad Amin TABATABAIEFAR ; Morteza HASHEMZADEH-CHALESHTORI

Journal of Audiology & Otology 2019;23(1):20-26

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