GJB2-话题@MedSci - 梅斯（MedSci）

#GJB2#

7篇内容 | 1014人围观

关注话题

话题活跃用户

#插入话题

插入图片

最新最热

[GetTopicListResponse(id=2063803, encodeId=9736206380337, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=Int J Pediatr Otorhinolaryngol：单个GJB2变异对兄弟姐妹听力水平影响的调查 , objectType=article, longId=215136, objectId=1c6b215136a9, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=1c6b215136a9, replyNumber=0, likeNumber=0, createdTime=2022-03-24, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=1c6b215136a9, moduleTitle=Int J Pediatr Otorhinolaryngol：单个GJB2变异对兄弟姐妹听力水平影响的调查 , moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=1c6b215136a9)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=2063802, encodeId=9ca62063802f0, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=Int J Pediatr Otorhinolaryngol：中国西北地区听力损失患者中GJB2、GJB3、SLC26A4和MT-RNR1变异频率研究, objectType=article, longId=198136, objectId=dd7a198136c6, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=dd7a198136c6, replyNumber=0, likeNumber=62, createdTime=2020-10-29, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=dd7a198136c6, moduleTitle=Int J Pediatr Otorhinolaryngol：中国西北地区听力损失患者中GJB2、GJB3、SLC26A4和MT-RNR1变异频率研究, moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=dd7a198136c6)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=2063800, encodeId=daed206380071, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=JCLA：有必要通过GJB3/GJB6筛查原发性听力损失GJB2携带者吗？, objectType=article, longId=158349, objectId=e72915834945, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=e72915834945, replyNumber=0, likeNumber=59, createdTime=2019-02-26, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=e72915834945, moduleTitle=JCLA：有必要通过GJB3/GJB6筛查原发性听力损失GJB2携带者吗？, moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=e72915834945)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=2063799, encodeId=d1142063e9981, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=Genet Test Mol Biomarkers：中国河南省非综合症听力损失儿童中GJB2、SLC26A4、MT-RNA1、和GJB3变异分析, objectType=article, longId=157970, objectId=4dd415e970a0, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=4dd415e970a0, replyNumber=0, likeNumber=65, createdTime=2019-03-20, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=4dd415e970a0, moduleTitle=Genet Test Mol Biomarkers：中国河南省非综合症听力损失儿童中GJB2、SLC26A4、MT-RNA1、和GJB3变异分析, moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=4dd415e970a0)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=2063798, encodeId=6b5a2063e982e, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=Eur Arch Otorhinolaryngol：GJB2变异以及临床表现分析, objectType=article, longId=146625, objectId=b2741466250f, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=b2741466250f, replyNumber=0, likeNumber=69, createdTime=2019-07-11, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=b2741466250f, moduleTitle=Eur Arch Otorhinolaryngol：GJB2变异以及临床表现分析, moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=b2741466250f)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=2063801, encodeId=56eb2063801ad, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=Genet Mol Biol：GJB2 c.235delC变异与常染色体隐性非综合征性听力损失和听神经病谱系障碍相关, objectType=article, longId=161693, objectId=fe4916169315, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=fe4916169315, replyNumber=0, likeNumber=90, createdTime=2019-07-17, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=fe4916169315, moduleTitle=Genet Mol Biol：GJB2 c.235delC变异与常染色体隐性非综合征性听力损失和听神经病谱系障碍相关, moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=fe4916169315)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=2063797, encodeId=150f2063e97bc, content=<a href='/topic/show?id=334b8040f3' target=_blank style='color:#2F92EE;'>#GJB2#</a>, objectTitle=J Hum Genet：俄罗斯GJB2/DFNB1突变谱更新：一个奠基性印古什人缺失突变(GJB2-D13S175)在其他大缺失突变中是频率更高的, objectType=article, longId=96043, objectId=da099604333, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=da099604333, replyNumber=0, likeNumber=62, createdTime=2017-06-25, rootId=0, userName=小刀医生, userId=8306486, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=da099604333, moduleTitle=J Hum Genet：俄罗斯GJB2/DFNB1突变谱更新：一个奠基性印古什人缺失突变(GJB2-D13S175)在其他大缺失突变中是频率更高的, moduleType=article, hrefUrl=//m.capotfarm.com/article/show_article.do?id=da099604333)], followStatus=false, userIsMember=false, type=1, lengthMark=0)] 梅斯话题小助手

GJB2

2020-05-29

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

Int J Pediatr Otorhinolaryngol：单个GJB2变异对兄弟姐妹听力水平影响的调查

2022-03-24

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

Int J Pediatr Otorhinolaryngol：中国西北地区听力损失患者中GJB2、GJB3、SLC26A4和MT-RNR1变异频率研究

2020-10-29

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

JCLA：有必要通过GJB3/GJB6筛查原发性听力损失GJB2携带者吗？

2019-02-26

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

Genet Test Mol Biomarkers：中国河南省非综合症听力损失儿童中GJB2、SLC26A4、MT-RNA1、和GJB3变异分析

2019-03-20

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

Eur Arch Otorhinolaryngol：GJB2变异以及临床表现分析

2019-07-11

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

Genet Mol Biol：GJB2 c.235delC变异与常染色体隐性非综合征性听力损失和听神经病谱系障碍相关

2019-07-17

小刀医生 (审核中...)

前往app查看评论内容

#GJB2#

J Hum Genet：俄罗斯GJB2/DFNB1突变谱更新：一个奠基性印古什人缺失突变(GJB2-D13S175)在其他大缺失突变中是频率更高的

2017-06-25

科室
- - 订阅+
  - 更多科室
工具
服务