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新生儿聋病基因筛查--悄然的革命 被引量:56

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作者 王秋菊
出处 《听力学及言语疾病杂志》 CAS CSCD 2008年第2期83-88,共6页 Journal of Audiology and Speech Pathology
基金 国家863项目(2006AA02Z181) 国家自然基金面上项目(30572016,30672310,30771203) 高等学校全国优秀博士学位论文作者专项资金资助项目(200463) 北京市科技计划重大项目(D0906005040291) 国家973项目(2007CB507400) 北京市重大专项课题项目(7070002)联合资助
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参考文献38

  • 1Harrison MJR, Wallace J. Trends in age of identification and intervention in infants with hearing loss[J]. Ear Hear, 2003, 24:89.
  • 2White KR. The current status of EHDI programs in the United States[J]. Ment Retard Dev Disabil Res Rev,2003, 9:79.
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  • 5Norris VW, Arnos KS, Hanks WD,et al. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness [J]. Ear Hear, 2006,27-732.
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  • 9聂文英,宫露霞,刘玉俊,相丽丽,林倩,戚以胜,聂迎玖.10501例新生儿听力筛查结果[J].中华医学杂志,2003,83(4):274-277. 被引量:86
  • 10余红,沈沛,赵军.7040例新生儿听力筛查结果分析[J].中国农村卫生事业管理,2004,24(3):61-62. 被引量:10

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