出处
《听力学及言语疾病杂志》
CAS
CSCD
2008年第2期158-160,共3页
Journal of Audiology and Speech Pathology
基金
国家自然科学基金资助项目(编号30572015)
参考文献24
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同被引文献35
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1戴朴,刘新,于飞,朱庆文,袁永一,杨淑芝,孙勍,袁慧军,杨伟炎,黄德亮,韩东一.18个省市聋校学生非综合征性聋病分子流行病学研究(Ⅰ)-GJB2 235delC和线粒体DNA 12SrRNA A1555G突变筛查报告[J].中华耳科学杂志,2006,4(1):1-5. 被引量：167
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2管敏鑫,赵立东.与氨基糖甙类抗生素耳毒性相关的线粒体12S rRNA突变的流行病学特征[J].中华耳科学杂志,2006,4(2):98-105. 被引量：72
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3张劲,李琦,戴朴,唐亮,刘新,阿衣木,欧阳星火,张昕,袁永一,朱庆文,金政策,李梅,薛丹丹.乌鲁木齐市特教学校重度感音神经性聋GJB2和线粒体基因常见突变调查[J].中华耳科学杂志,2007,5(1):60-63. 被引量：8
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引证文献2
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1盛国强,徐红霞,李彦华.新疆维吾尔族遗传性聋非综合征型GJB2基因突变与中医证型的关系[J].新中医,2013,45(6):101-102. 被引量：1
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2蔡小牛,李彦华,罗永海,邹广华,汪常伟.非综合征型遗传性聋与GJB2的研究近况及新疆地区的研究进展[J].中国中西医结合耳鼻咽喉科杂志,2014,22(1):77-80. 被引量：1
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1刘光华.难治性鼻出血60例临床分析[J].中国医药导报,2009,6(5):147-147. 被引量：3
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2陈迟,徐百成,郭玉芬.大前庭水管综合征诊断进展及防治[J].国际耳鼻咽喉头颈外科杂志,2015,39(3):170-174. 被引量：2
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3高东梅,刘洪泉,金鹏,于姝媛,王苹,杜波.30例大前庭水管综合征患者SLC26A4基因诊断与听性脑干电位特性分析[J].中国实验诊断学,2016,20(9):1586-1589.
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4常青.常染色体隐性非综合征性听力减退[J].国外医学（耳鼻咽喉科学分册）,2001,25(6):353-356.
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5阿布利克木.依明,唐亮,张劲.大前庭水管综合征的相关研究进展[J].临床耳鼻咽喉头颈外科杂志,2012,26(22):1049-1053. 被引量：4
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6郝爱华,李昌玲.持续气道正压通气治疗OSAS合并难治性高血压临床观察[J].山东医药,2008,48(27):47-47. 被引量：1
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7欧阳治国,金舰,陈家海.一个非综合征型聋家系的分子病因学研究[J].听力学及言语疾病杂志,2015,23(5):485-488.
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8黎燕群,张希龙.阻塞性睡眠呼吸暂停综合征与难治性高血压相关性研究进展[J].国际呼吸杂志,2008,28(3):161-164. 被引量：2
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9徐聪,陆家海.连接蛋白与遗传性耳聋研究现状和基因治疗的研究展望[J].热带医学杂志,2007,7(4):393-395.
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10崔庆佳,黄丽辉.GJB2基因突变与听力损失的关系[J].临床耳鼻咽喉头颈外科杂志,2013,27(19):1099-1102. 被引量：6
