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Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss
Wang Rongrong; Han Shirui; Khan Amjad; Zhang Xue
2017
卷号21期号:5页码:316-321
关键词hearing loss gene mutation targeted next-generation sequencing whole-exome sequencing
ISSN号1945-0265
DOI10.1089/gtmb.2016.0328
URL标识查看原文
收录类别SCIE ; PUBMED
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/6367679
专题中国医学科学院 北京协和医学院
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GB/T 7714
Wang Rongrong,Han Shirui,Khan Amjad,et al. Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss[J],2017,21(5):316-321.
APA Wang Rongrong,Han Shirui,Khan Amjad,&Zhang Xue.(2017).Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.,21(5),316-321.
MLA Wang Rongrong,et al."Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss".21.5(2017):316-321.
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