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Publications by Fatemeh Azadegan‐Dehkordi
GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations
Annals of Human Genetics
Genetics
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Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population
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Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population
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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
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Pathophysiology of Age-Related Hearing Loss (Peripheral and Central)
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Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment
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