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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
Fatemeh Azadegan-Dehkordi, Tayyebe Bahrami, Maryam Shirzad, Gelareh Karbasi, Nasrin Yazdanpanahi, Effat Farrokhi, Mahbobeh Koohiyan, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh-Chaleshtori
J Audiol Otol. 2019;23(1):20-26.   Published online December 7, 2018
DOI: https://doi.org/10.7874/jao.2018.00185

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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
Journal of Audiology and Otology. 2019;23(1):20-26   Crossref logo
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Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness
International Journal of Pediatric Otorhinolaryngology. 2007;71(6):869-873   Crossref logo
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GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss
Human Mutation. 2002;19(5):572-572   Crossref logo
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The frequency of GJB2 mutations and the Δ (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population
Clinical Genetics. 2004;65(6):506-508   Crossref logo
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GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation
International Journal of Pediatric Otorhinolaryngology. 2007;71(8):1239-1245   Crossref logo
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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants
International Journal of Pediatric Otorhinolaryngology. 2018;107:121-126   Crossref logo
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Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3
International Journal of Pediatric Otorhinolaryngology. 2013;77(2):189-193   Crossref logo
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Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss
Clinical Genetics. 2003;64(1):65-69   Crossref logo
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The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family
Clinical Genetics. 2002;62(4):306-309   Crossref logo
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Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran
International Journal of Pediatric Otorhinolaryngology. 2015;79(11):1892-1895   Crossref logo
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