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Correlation analysis of genotypes, auditory function, and vestibular size in Chinese children with enlarged vestibular aqueduct syndrome

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Pages 1242-1249 | Received 07 May 2013, Accepted 30 Jun 2013, Published online: 19 Nov 2013

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Articles from other publishers (13)

Emilio Avallone, Pietro De Luca, Pasquale Viola, Massimo Ralli, Federico Maria Gioacchini, Giuseppe Chiarella, Filippo Ricciardiello, Claudia Cassandro, Giovanni Salzano, Thomas Lenarz, Francesco Antonio Salzano & Alfonso Scarpa. (2023) Correlation Between Air–Bone Gap and Vestibular Aqueduct Size in Enlarged Vestibular Aqueduct Syndrome: A Systematic Review. Indian Journal of Otolaryngology and Head & Neck Surgery.
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Natalia Bałdyga, Dominika Oziębło, Nina Gan, Mariusz Furmanek, Marcin L. Leja, Henryk Skarżyński & Monika Ołdak. (2023) The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 14:2, pages 335.
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K. Bouhadjer, L.V. Romo, M.J. Brennan, B.M. Kozak, E. Hattingen, A.F. Juliano, H.D. Curtin & K.L. Reinshagen. (2023) Retrospective Analysis of the Association of a Small Vestibular Aqueduct with Cochleovestibular Symptoms in a Large, Single-Center Cohort Undergoing CT. American Journal of Neuroradiology 44:1, pages 70-73.
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Keiji Honda & Andrew J. Griffith. (2021) Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss. Human Genetics 141:3-4, pages 455-464.
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Akira Ganaha, Eiji Hishinuma, Tadashi Kaname, Masahiro Hiratsuka, Shunsuke Kondo & Tetsuya Tono. (2022) Rapid Genetic Diagnosis for Okinawan Patients with Enlarged Vestibular Aqueduct Using Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip. Journal of Clinical Medicine 11:4, pages 1099.
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K. Bouhadjer, K. Tissera, C.W. Farris, A.F Juliano, M.E. Cunnane, H.D. Curtin, L.A. Mankarious & K.L. Reinshagen. (2021) Retrospective Review of Midpoint Vestibular Aqueduct Size in the 45° Oblique (Pöschl) Plane and Correlation with Hearing Loss in Patients with Enlarged Vestibular Aqueduct. American Journal of Neuroradiology 42:12, pages 2215-2221.
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Andrew J. Griffith & Keiji Honda. 2021. Cummings Pediatric Otolaryngology. Cummings Pediatric Otolaryngology 201 209 .
Cheng WenShijie WangXuelei ZhaoXianlei WangXueyao WangXiaohua ChengLihui Huang. (2019) Mutation analysis of the <i>SLC26A4</i> gene in three Chinese families. BioScience Trends 13:5, pages 441-447.
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Yongbo Yu, Yang Yang, Jie Lu, Yaqiong Jin, Yeran Yang, Enyu Hong, Jin Shi, Feng Chen, Shujing Han, Ping Chu, Yongli Guo & Xin Ni. (2019) Two Compound Heterozygous Were Identified in <i>SLC26A4</i> Gene in Two Chinese Families With Enlarged Vestibular Aqueduct. Clinical and Experimental Otorhinolaryngology 12:1, pages 50-57.
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Xuelei Zhao, Xiaohua Cheng, Lihui Huang, Xianlei Wang, Cheng Wen & Xueyao Wang. (2018) Novel compound heterozygous mutations in <i>SLC26A4</i> gene in a Chinese family with enlarged vestibular aqueduct. BioScience Trends 12:5, pages 502-506.
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Mingming Wang, Fengguo Zhang, Lei Xu, Yun Xiao, Jianfeng Li, Zhaomin Fan, Qian Sun, Xiaohui Bai & Haibo Wang. (2016) Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct. International Journal of Pediatric Otorhinolaryngology 90, pages 170-174.
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W.F. Burke. (2015) Hereditäre SchwerhörigkeitHereditary hearing loss. Humanmedizin kompakt.
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W.F. Burke, T. Lenarz & H. Maier. (2014) Hereditäre SchwerhörigkeitHereditary hearing loss. HNO 62:10, pages 759-770.
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