PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Journal of Audiology and Otology10.7874/jao.2019.000592019234175-180Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 MutationsMahbobeh Koohiyan, Fatemeh Azadegan-Dehkordi, Farideh Koohian, Morteza Hashemzadeh-Chaleshtorihttp://ejao.org/upload/pdf/jao-2019-00059.pdf, http://ejao.org/journal/view.php?doi=10.7874/jao.2019.00059, http://ejao.org/upload/pdf/jao-2019-00059.pdf
Annals of Human Genetics10.1111/ahg.123542019842107-113GJB2‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutationsMahbobeh Koohiyan, Farideh Koohian, Fatemeh Azadegan‐Dehkordihttps://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12354, https://onlinelibrary.wiley.com/doi/full-xml/10.1111/ahg.12354, https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12354
Annals of Human Genetics10.1111/ahg.120622014783235-242Update of the Spectrum ofGJB2Mutations in 107 Patients with Nonsyndromic Hearing Loss in the Fujian Population of ChinaTianbin Chen, Ling Jiang, Can Liu, Hongyan Shan, Jing Chen, Bin Yang, Qishui Ouhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fahg.12062, http://onlinelibrary.wiley.com/wol1/doi/10.1111/ahg.12062/fullpdf
Human Genetics10.1007/s00439-002-0762-y20021112145-153Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in AustriaAndreas R. Janecke, Almut Hirst-Stadlmann, Barbara Günther, Barbara Utermann, Thomas Müller, Judith Löffler, Gerd Utermann, Doris Nekahm-Heishttp://link.springer.com/content/pdf/10.1007/s00439-002-0762-y.pdf, http://link.springer.com/article/10.1007/s00439-002-0762-y/fulltext.html, http://link.springer.com/content/pdf/10.1007/s00439-002-0762-y
International Journal of Pediatric Otorhinolaryngology10.1016/j.ijporl.2019.01.0362019119136-140An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature reviewMahbobeh koohiyan, Amirhossein Ahmadi, Farideh koohian, Shahrzad Aghaei, Beheshteh Amiri, Morteza Hashemzadeh-Chaleshtorihttps://api.elsevier.com/content/article/PII:S0165587619300473?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0165587619300473?httpAccept=text/plain
Hearing Research10.1016/j.heares.2020.1081352022413108135GJB2 mutation spectrum in the Taiwanese population and genotype–phenotype comparisons in patients with hearing loss carrying GJB2 c.109G>A and c.235delC mutationsYi-Feng Lin, Hung-Ching Lin, Chia-Ling Tsai, Yi-Chao Hsuhttps://api.elsevier.com/content/article/PII:S0378595520304068?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0378595520304068?httpAccept=text/plain
Clinical Genetics10.1111/j.1399-0004.2004.00233.x2004654338-342The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defectsT Fitzgerald, S Duva, H Ostrer, K Pass, C Oddoux, R Ruben, M Cagganahttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.2004.00233.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00233.x/fullpdf
Annals of Human Genetics10.1111/ahg.1228420188311-10Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing lossFatemeh Azadegan‐Dehkordi, Reza Ahmadi, Mahbobeh Koohiyan, Morteza Hashemzadeh‐Chaleshtorihttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fahg.12284, https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12284, https://onlinelibrary.wiley.com/doi/full-xml/10.1111/ahg.12284, https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12284
International Journal of Pediatric Otorhinolaryngology10.1016/j.ijporl.2008.11.0102009733437-443High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, IndiaAnu Yamuna Joseph, T.J. Rasoolhttps://api.elsevier.com/content/article/PII:S0165587608005776?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S0165587608005776?httpAccept=text/plain
Clinical Genetics10.1111/j.1399-0004.2005.00529.x2005686554-557GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysishttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.2005.00529.x, http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.00529.x/fullpdf