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Diagnostic pitfalls for GJB2 -related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss

机译：GJB2相关听力损失的诊断陷阱：日本患者中的阵列 - CGH分析检测到先天性深刻听力损失的新型缺失

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Satoko Abe; Shin-ya Nishio; Yoh Yokota; Hideaki Moteki; Kozo Kumakawa; Shin-ichi Usami;
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1. Diagnostic pitfalls for GJB2 ‐related hearing loss: A novel deletion detected by Array‐CGH analysis in a Japanese patient with congenital profound hearing loss [J] . Satoko Abe, Shin‐ya Nishio, Yoh Yokota, Clinical Case Reports . 2018,第11期

机译：GJB2相关性听力损失的诊断陷阱：通过Array-CGH分析检测到的日本先天性重度听力损失患者的新型缺失
2. Changes in the connexin 26 gene (GJB2) in Russian patients with hearing loss: Results of long-term molecular diagnostics of hereditary nonsyndromic hearing loss [J] . Bliznetz E.A., Galkina V.A., Matyushchenko G.N., Russian journal of genetics . 2012,第1期

机译：俄罗斯听力丧失患者连接蛋白26基因（GJB2）的变化：遗传性非综合征性听力丧失的长期分子诊断结果
3. Analysis of the GJB2 and GJB6 Genes in Italian Patients with Nonsyndromic Hearing Loss: Frequencies,Novel Mutations, Genotypes, and Degree of Hearing Loss [J] . Paola Primignani, Luca Trotta, Pierangela Castorina, Genetic Testing . 2009,第2期

机译：非综合征性听力损失的意大利患者中GJB2和GJB6基因的分析：频率，小说突变，基因型和听力损失的程度
4. A New Hearing Aid Fitting Strategy for Severe to Profound Hearing Loss [C] . Herzke Tobias, Haumann Sabine, Hohmann Volker Proceedings of Speech Communication; 10. ITG Symposium. . 2012

机译：重度严重失聪的新型助听器适配策略
5. A micro-ethnographic study of communication/language development in a Japanese child with profound hearing loss before and after cochlear implantation. [D] . Kuwahara, Katsura. 2008

机译：一项微民族志研究，研究了日本儿童在人工耳蜗植入前后的严重听力损失，其交流/语言发展情况。
6. Diagnostic pitfalls for GJB2‐related hearing loss: A novel deletion detected by Array‐CGH analysis in a Japanese patient with congenital profound hearing loss [O] . Satoko Abe, Shin‐ya Nishio, Yoh Yokota, 2018

机译：GJB2相关性听力损失的诊断陷阱：通过Array-CGH分析在日本先天性重度听力损失患者中发现的一种新型缺失
7. Analysis of GJB2 (Connexin 26) Mutation in Patients with Congenital Non-Syndromic Sensorineural Hearing Loss [O] . Emin Kaskalan, Ebru Etem Önalan, İrfan Kaygusuz, 2015

机译：先天性非综合征性感音神经性听力损失患者GJB2（连接蛋白26）突变分析

Diagnostic pitfalls for GJB2 -related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing loss

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