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Publications by Farideh Koohian
GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations
Annals of Human Genetics
Genetics
Related publications
Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population
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GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss
Revista Romana de Medicina de Laborator
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
International Journal of Pediatric Otorhinolaryngology
Medicine
Otorhinolaryngology
Pediatrics
Perinatology
Child Health
Prevalence of Cx26 (GJB2) Gene Mutations Causing Recessive Nonsyndromic Hearing Impairment in India
International Journal of Human Genetics
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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)
Korean Journal of Audiology
Frequency of GJB 2 Mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 Deletions Among Patients With Non‐syndromic Hearing Loss From the Central Region of Iran
Molecular genetics & genomic medicine
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Molecular Biology
Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment
Genetics Research International
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Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss
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