遗传性-话题@MedSci

#遗传性#

276篇内容 | 2233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=1860192, encodeId=4a91186019298, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Cell Reports Medicine：遗传性阴道细菌影响免疫耐受，并与婴儿期变应性致敏的早期标志物相关, objectType=article, longId=736161, objectId=f382e3616166, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=f382e3616166, replyNumber=0, likeNumber=123, createdTime=2023-02-26, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=f382e3616166, moduleTitle=Cell Reports Medicine：遗传性阴道细菌影响免疫耐受，并与婴儿期变应性致敏的早期标志物相关, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=f382e3616166)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860191, encodeId=78e11860191f4, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Neurology：遗传性额颞叶痴呆，长期认知功能如何变化？, objectType=article, longId=735201, objectId=c1c5e3520144, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=c1c5e3520144, replyNumber=0, likeNumber=123, createdTime=2023-04-15, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=c1c5e3520144, moduleTitle=Neurology：遗传性额颞叶痴呆，长期认知功能如何变化？, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=c1c5e3520144)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860184, encodeId=b19b186018499, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=NEJM发布遗传性肝病RNAi疗法2期临床试验结果，降低致病蛋白83%, objectType=article, longId=730942, objectId=b578e309426a, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=b578e309426a, replyNumber=0, likeNumber=175, createdTime=2022-07-13, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=b578e309426a, moduleTitle=NEJM发布遗传性肝病RNAi疗法2期临床试验结果，降低致病蛋白83%, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=b578e309426a)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860182, encodeId=00e11860182fa, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=BMC Medical Genomics：遗传性耳聋最新研究成果：复旦团队通过WGS锁定新型拷贝数变异缺失, objectType=article, longId=728903, objectId=b1a9e28903c0, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=b1a9e28903c0, replyNumber=0, likeNumber=127, createdTime=2022-08-29, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=b1a9e28903c0, moduleTitle=BMC Medical Genomics：遗传性耳聋最新研究成果：复旦团队通过WGS锁定新型拷贝数变异缺失, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=b1a9e28903c0)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860195, encodeId=63cc1860195b0, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=重大进展！两篇Science论文发现与病毒感染和遗传性代谢疾病相关的关键蛋白, objectType=article, longId=739137, objectId=9da1e39137a4, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=9da1e39137a4, replyNumber=0, likeNumber=119, createdTime=2023-07-23, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=9da1e39137a4, moduleTitle=重大进展！两篇Science论文发现与病毒感染和遗传性代谢疾病相关的关键蛋白, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=9da1e39137a4)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860186, encodeId=0be1186018676, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=CPR：首次证实，膳食补充剂可以预防遗传性癌症, objectType=article, longId=733570, objectId=545ae3357077, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=545ae3357077, replyNumber=0, likeNumber=148, createdTime=2023-05-02, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=545ae3357077, moduleTitle=CPR：首次证实，膳食补充剂可以预防遗传性癌症, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=545ae3357077)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860183, encodeId=dd59186018393, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=FDA批准vutrisiran治疗成人遗传性转甲状腺素蛋白淀粉样变性伴多发性神经病（hATTR-PN），这是第5款siRNA药物, objectType=article, longId=729775, objectId=6f41e29775b5, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=6f41e29775b5, replyNumber=0, likeNumber=117, createdTime=2023-04-29, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=6f41e29775b5, moduleTitle=FDA批准vutrisiran治疗成人遗传性转甲状腺素蛋白淀粉样变性伴多发性神经病（hATTR-PN），这是第5款siRNA药物, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=6f41e29775b5)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860178, encodeId=6fb018601e823, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Nat Commun：体内单碱基编辑，一次性持久治疗遗传性失明, objectType=article, longId=723660, objectId=eab0e236604a, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=eab0e236604a, replyNumber=0, likeNumber=105, createdTime=2022-04-17, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=eab0e236604a, moduleTitle=Nat Commun：体内单碱基编辑，一次性持久治疗遗传性失明, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=eab0e236604a)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860181, encodeId=0dad1860181c4, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=JAMA Cardiol：遗传性心肌病相关致病性变异与心血管疾病和全因死亡率的相关性, objectType=article, longId=727961, objectId=21d8e279617e, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=21d8e279617e, replyNumber=0, likeNumber=141, createdTime=2023-03-16, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=21d8e279617e, moduleTitle=JAMA Cardiol：遗传性心肌病相关致病性变异与心血管疾病和全因死亡率的相关性, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=21d8e279617e)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860188, encodeId=200f1860188ae, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Neurology：惯性步态传感器测量遗传性痉挛性截瘫患者的活动性和功能:一项横断面多中心临床研究, objectType=article, longId=733905, objectId=43b8e3390532, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=43b8e3390532, replyNumber=0, likeNumber=143, createdTime=2023-06-03, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=43b8e3390532, moduleTitle=Neurology：惯性步态传感器测量遗传性痉挛性截瘫患者的活动性和功能:一项横断面多中心临床研究, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=43b8e3390532)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860180, encodeId=40b318601800b, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=npj Parkinsons Dis：遗传性研究新发现，帕金森和脂质代谢密切相关, objectType=article, longId=723929, objectId=3be0e23929dc, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=3be0e23929dc, replyNumber=0, likeNumber=106, createdTime=2022-12-26, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=3be0e23929dc, moduleTitle=npj Parkinsons Dis：遗传性研究新发现，帕金森和脂质代谢密切相关, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=3be0e23929dc)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860177, encodeId=43fb18601e788, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Stroke：老年脑出血主要病因——遗传性CAA磁共振标志物和认知能力的纵向发展情况, objectType=article, longId=723405, objectId=78dce23405a7, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=78dce23405a7, replyNumber=0, likeNumber=145, createdTime=2023-02-12, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=78dce23405a7, moduleTitle=Stroke：老年脑出血主要病因——遗传性CAA磁共振标志物和认知能力的纵向发展情况, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=78dce23405a7)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860194, encodeId=fe261860194d1, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=遗传性大疱性表皮松解症（蝴蝶宝贝）：症状与体征、病因、流行病学、诊断与治疗, objectType=article, longId=736398, objectId=fc6ae3639863, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=fc6ae3639863, replyNumber=0, likeNumber=115, createdTime=2022-11-01, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=fc6ae3639863, moduleTitle=遗传性大疱性表皮松解症（蝴蝶宝贝）：症状与体征、病因、流行病学、诊断与治疗, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=fc6ae3639863)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860168, encodeId=366e186016873, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=ProQR的RNA疗法在关键的遗传性眼病研究中失败, objectType=article, longId=295606, objectId=befe29560674, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=befe29560674, replyNumber=0, likeNumber=157, createdTime=2022-02-17, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=befe29560674, moduleTitle=ProQR的RNA疗法在关键的遗传性眼病研究中失败, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=befe29560674)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860175, encodeId=eee218601e543, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Alzheimers Dementia：遗传性痴呆，蓝斑核完整性降低，随后tau聚集增加, objectType=article, longId=301388, objectId=36fd301388da, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=36fd301388da, replyNumber=0, likeNumber=167, createdTime=2022-12-02, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=36fd301388da, moduleTitle=Alzheimers Dementia：遗传性痴呆，蓝斑核完整性降低，随后tau聚集增加, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=36fd301388da)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860179, encodeId=79ab18601e947, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Haematologica：诱发白血病的综合征是儿童遗传性血细胞减少症的主要原因, objectType=article, longId=723685, objectId=1aa2e23685e4, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=1aa2e23685e4, replyNumber=0, likeNumber=102, createdTime=2022-09-20, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=1aa2e23685e4, moduleTitle=Haematologica：诱发白血病的综合征是儿童遗传性血细胞减少症的主要原因, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=1aa2e23685e4)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860193, encodeId=ca5818601934c, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=2022年浙江省家族遗传性肿瘤论坛, objectType=article, longId=736326, objectId=96f5e3632675, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=96f5e3632675, replyNumber=0, likeNumber=124, createdTime=2022-08-22, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=96f5e3632675, moduleTitle=2022年浙江省家族遗传性肿瘤论坛, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=96f5e3632675)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860187, encodeId=588f186018ea5, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=首次证实，膳食补充剂可以预防遗传性癌症, objectType=article, longId=733646, objectId=5ceae33646da, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=5ceae33646da, replyNumber=0, likeNumber=128, createdTime=2023-05-20, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=5ceae33646da, moduleTitle=首次证实，膳食补充剂可以预防遗传性癌症, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=5ceae33646da)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860176, encodeId=8e1018601e6ea, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=林志淼教授：遗传性大疱性表皮松解症的临床表现及疾病诊断, objectType=article, longId=301840, objectId=ffe2301840f8, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=ffe2301840f8, replyNumber=0, likeNumber=122, createdTime=2022-07-25, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=ffe2301840f8, moduleTitle=林志淼教授：遗传性大疱性表皮松解症的临床表现及疾病诊断, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=ffe2301840f8)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1860167, encodeId=f44e186016e21, content=<a href='/topic/show?id=cc73951054b' target=_blank style='color:#2F92EE;'>#遗传性#</a>, objectTitle=Lancet子刊：遗传性阿尔茨海默病Aβ的水平异质性, objectType=article, longId=294873, objectId=7d742948e3c2, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=7d742948e3c2, replyNumber=0, likeNumber=117, createdTime=2022-04-23, rootId=0, userName=般若傻瓜, userId=ad9f79, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=7d742948e3c2, moduleTitle=Lancet子刊：遗传性阿尔茨海默病Aβ的水平异质性, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=7d742948e3c2)], followStatus=false, userIsMember=false, type=1, lengthMark=0)] 梅斯话题小助手

遗传性

2020-05-29

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Cell Reports Medicine：遗传性阴道细菌影响免疫耐受，并与婴儿期变应性致敏的早期标志物相关

2023-02-26

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Neurology：遗传性额颞叶痴呆，长期认知功能如何变化？

2023-04-15

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

NEJM发布遗传性肝病RNAi疗法2期临床试验结果，降低致病蛋白83%

2022-07-13

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

BMC Medical Genomics：遗传性耳聋最新研究成果：复旦团队通过WGS锁定新型拷贝数变异缺失

2022-08-29

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

重大进展！两篇Science论文发现与病毒感染和遗传性代谢疾病相关的关键蛋白

2023-07-23

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

CPR：首次证实，膳食补充剂可以预防遗传性癌症

2023-05-02

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

FDA批准vutrisiran治疗成人遗传性转甲状腺素蛋白淀粉样变性伴多发性神经病（hATTR-PN），这是第5款siRNA药物

2023-04-29

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Nat Commun：体内单碱基编辑，一次性持久治疗遗传性失明

2022-04-17

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

JAMA Cardiol：遗传性心肌病相关致病性变异与心血管疾病和全因死亡率的相关性

2023-03-16

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Neurology：惯性步态传感器测量遗传性痉挛性截瘫患者的活动性和功能:一项横断面多中心临床研究

2023-06-03

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

npj Parkinsons Dis：遗传性研究新发现，帕金森和脂质代谢密切相关

2022-12-26

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Stroke：老年脑出血主要病因——遗传性CAA磁共振标志物和认知能力的纵向发展情况

2023-02-12

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

遗传性大疱性表皮松解症（蝴蝶宝贝）：症状与体征、病因、流行病学、诊断与治疗

2022-11-01

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

ProQR的RNA疗法在关键的遗传性眼病研究中失败

2022-02-17

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Alzheimers Dementia：遗传性痴呆，蓝斑核完整性降低，随后tau聚集增加

2022-12-02

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Haematologica：诱发白血病的综合征是儿童遗传性血细胞减少症的主要原因

2022-09-20

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

2022年浙江省家族遗传性肿瘤论坛

2022-08-22

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

首次证实，膳食补充剂可以预防遗传性癌症

2023-05-20

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

林志淼教授：遗传性大疱性表皮松解症的临床表现及疾病诊断

2022-07-25

般若傻瓜 (审核中...)

前往app查看评论内容

#遗传性#

Lancet子刊：遗传性阿尔茨海默病Aβ的水平异质性

2022-04-23

科室
- - 订阅+
  - 更多科室
工具
服务