染色体-话题@MedSci

#染色体#

194篇内容 | 2264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=1331712, encodeId=d4a21331e126a, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=IJLH：219例伴有染色体异常和/或酪氨酸激酶域突变的慢性髓样白血病患者的结局, objectType=article, longId=167566, objectId=1e3c16e56624, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=1e3c16e56624, replyNumber=0, likeNumber=62, createdTime=2019-06-04, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=1e3c16e56624, moduleTitle=IJLH：219例伴有染色体异常和/或酪氨酸激酶域突变的慢性髓样白血病患者的结局, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=1e3c16e56624)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331711, encodeId=b92f1331e116b, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=前列腺癌治还是不治？染色体可以告诉你答案, objectType=article, longId=166780, objectId=b391166e8079, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=b391166e8079, replyNumber=0, likeNumber=57, createdTime=2019-05-26, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=b391166e8079, moduleTitle=前列腺癌治还是不治？染色体可以告诉你答案, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=b391166e8079)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331710, encodeId=955f1331e102e, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Lancet：Burosumab可明显改善X染色体连锁的低磷血症患儿的佝偻病表现, objectType=article, longId=166503, objectId=1b191665036b, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=1b191665036b, replyNumber=0, likeNumber=78, createdTime=2019-05-22, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=1b191665036b, moduleTitle=Lancet：Burosumab可明显改善X染色体连锁的低磷血症患儿的佝偻病表现, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=1b191665036b)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331709, encodeId=9d641331e09ca, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=JCLA：利用染色体微阵列分析检测拷贝数变异--用于先天性心脏缺陷的产前诊断, objectType=article, longId=166244, objectId=6d3b16624483, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=6d3b16624483, replyNumber=0, likeNumber=82, createdTime=2019-05-18, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=6d3b16624483, moduleTitle=JCLA：利用染色体微阵列分析检测拷贝数变异--用于先天性心脏缺陷的产前诊断, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=6d3b16624483)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331708, encodeId=6b9d1331e0899, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=NEJM：累积肝脏的常染色体显性遗传多囊肾病-病例报道, objectType=article, longId=166193, objectId=869f16619364, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=869f16619364, replyNumber=0, likeNumber=79, createdTime=2019-05-17, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=869f16619364, moduleTitle=NEJM：累积肝脏的常染色体显性遗传多囊肾病-病例报道, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=869f16619364)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331707, encodeId=a4771331e07e7, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=ARCH PATHOL LAB MED：染色体基因组阵列检测在未分类晚期肾细胞癌中的临床应用, objectType=article, longId=165773, objectId=03bd165e73c2, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=03bd165e73c2, replyNumber=0, likeNumber=72, createdTime=2019-05-11, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=03bd165e73c2, moduleTitle=ARCH PATHOL LAB MED：染色体基因组阵列检测在未分类晚期肾细胞癌中的临床应用, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=03bd165e73c2)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331706, encodeId=eda71331e06ce, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=NAT GENET：人类结直肠癌类器官染色体不稳定性和核型进化过程, objectType=article, longId=165306, objectId=a38116530658, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=a38116530658, replyNumber=0, likeNumber=53, createdTime=2019-05-04, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=a38116530658, moduleTitle=NAT GENET：人类结直肠癌类器官染色体不稳定性和核型进化过程, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=a38116530658)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331705, encodeId=3bd51331e05bb, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=BMC Med Genet：常染色体隐性非综合征听力损失患者中，MYO15A基因型表型相关性分析, objectType=article, longId=164871, objectId=59821648e18d, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=59821648e18d, replyNumber=0, likeNumber=59, createdTime=2019-04-25, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=59821648e18d, moduleTitle=BMC Med Genet：常染色体隐性非综合征听力损失患者中，MYO15A基因型表型相关性分析, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=59821648e18d)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331704, encodeId=5ccc1331e04ad, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</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=72, createdTime=2019-03-07, rootId=0, userName=新生儿张玉军, userId=38fd2500059, 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=https://www.medsci.cn/article/show_article.do?id=fe4916169315)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331703, encodeId=21031331e03f0, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=AGING CELL：男性Y染色体年龄依赖性DNA甲基化模式, objectType=article, longId=161477, objectId=72071614e7c4, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=72071614e7c4, replyNumber=0, likeNumber=106, createdTime=2019-03-02, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=72071614e7c4, moduleTitle=AGING CELL：男性Y染色体年龄依赖性DNA甲基化模式, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=72071614e7c4)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331702, encodeId=8b191331e02de, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=RARS型骨髓增生异常综合征患者伴有ph染色体阳性1例, objectType=article, longId=160658, objectId=0a5c16065817, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=0a5c16065817, replyNumber=0, likeNumber=66, createdTime=2019-02-22, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=0a5c16065817, moduleTitle=RARS型骨髓增生异常综合征患者伴有ph染色体阳性1例, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=0a5c16065817)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331701, encodeId=f57e1331e01a1, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=病例分享 | 慢性髓系白血病双费城染色体阳性同时表达P210BCR-ABL1和P195BCR-ABL1, objectType=article, longId=160191, objectId=ae36160191ca, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=ae36160191ca, replyNumber=0, likeNumber=53, createdTime=2019-02-18, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=ae36160191ca, moduleTitle=病例分享 | 慢性髓系白血病双费城染色体阳性同时表达P210BCR-ABL1和P195BCR-ABL1, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=ae36160191ca)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331700, encodeId=88651331e0093, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Haematologica：病例分享 | 慢性髓系白血病双费城染色体阳性同时表达P210BCR-ABL1和P195BCR-ABL1, objectType=article, longId=160125, objectId=f00f160125bf, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=f00f160125bf, replyNumber=0, likeNumber=66, createdTime=2019-02-17, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=f00f160125bf, moduleTitle=Haematologica：病例分享 | 慢性髓系白血病双费城染色体阳性同时表达P210BCR-ABL1和P195BCR-ABL1, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=f00f160125bf)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331699, encodeId=a05a133169920, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Biochem Genet：新型常染色体隐性视网膜色素病变CNGA1基因突变（c.G622A）导致膜上CNGA1蛋白质减少, objectType=article, longId=159296, objectId=d7251592963d, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=d7251592963d, replyNumber=0, likeNumber=34, createdTime=2019-02-02, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=d7251592963d, moduleTitle=Biochem Genet：新型常染色体隐性视网膜色素病变CNGA1基因突变（c.G622A）导致膜上CNGA1蛋白质减少, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=d7251592963d)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331698, encodeId=daa61331698aa, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Bardoxolone治疗常染色体显性多囊肾病的III期试验正式开始, objectType=article, longId=159160, objectId=1493159160dd, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=1493159160dd, replyNumber=0, likeNumber=79, createdTime=2019-01-30, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=1493159160dd, moduleTitle=Bardoxolone治疗常染色体显性多囊肾病的III期试验正式开始, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=1493159160dd)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331697, encodeId=dda3133169eb9, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=INT J LAB HEMATOL：219例慢性髓系白血病合并染色体异常和/或酪氨酸激酶域突变的结果, objectType=article, longId=159066, objectId=263d15906641, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=263d15906641, replyNumber=0, likeNumber=77, createdTime=2019-01-29, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=263d15906641, moduleTitle=INT J LAB HEMATOL：219例慢性髓系白血病合并染色体异常和/或酪氨酸激酶域突变的结果, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=263d15906641)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331696, encodeId=daae13316962c, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=NATURE：自噬性细胞死亡保护染色体稳定性, objectType=article, longId=158944, objectId=03651589448f, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=03651589448f, replyNumber=0, likeNumber=82, createdTime=2019-01-28, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=03651589448f, moduleTitle=NATURE：自噬性细胞死亡保护染色体稳定性, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=03651589448f)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331695, encodeId=988e1331695ed, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Nat Commun：是男，是女，可不是XY染色体说了算这么简单……, objectType=article, longId=156103, objectId=6a51156103fe, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=6a51156103fe, replyNumber=0, likeNumber=92, createdTime=2018-12-20, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=6a51156103fe, moduleTitle=Nat Commun：是男，是女，可不是XY染色体说了算这么简单……, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=6a51156103fe)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331694, encodeId=f11313316942e, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Eur Urol：Y染色体上LncRNA对前列腺癌的促进作用机制获进展, objectType=article, longId=155940, objectId=72b6155940a2, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=72b6155940a2, replyNumber=0, likeNumber=81, createdTime=2018-12-18, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=72b6155940a2, moduleTitle=Eur Urol：Y染色体上LncRNA对前列腺癌的促进作用机制获进展, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=72b6155940a2)], followStatus=false, userIsMember=false, type=1, lengthMark=0), GetTopicListResponse(id=1331693, encodeId=9ba1133169394, content=<a href='/topic/show?id=d85a6181e4d' target=_blank style='color:#2F92EE;'>#染色体#</a>, objectTitle=Eur J Med Genet：非综合征常染色体隐性听力损失的一个稀有变异-LHFPL5变异分析, objectType=article, longId=155035, objectId=0d08155035b3, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=0d08155035b3, replyNumber=0, likeNumber=52, createdTime=2018-12-05, rootId=0, userName=新生儿张玉军, userId=38fd2500059, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=0d08155035b3, moduleTitle=Eur J Med Genet：非综合征常染色体隐性听力损失的一个稀有变异-LHFPL5变异分析, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=0d08155035b3)], followStatus=false, userIsMember=false, type=1, lengthMark=0)] 梅斯话题小助手

染色体

2020-05-29

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

IJLH：219例伴有染色体异常和/或酪氨酸激酶域突变的慢性髓样白血病患者的结局

2019-06-04

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

前列腺癌治还是不治？染色体可以告诉你答案

2019-05-26

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Lancet：Burosumab可明显改善X染色体连锁的低磷血症患儿的佝偻病表现

2019-05-22

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

JCLA：利用染色体微阵列分析检测拷贝数变异--用于先天性心脏缺陷的产前诊断

2019-05-18

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

NEJM：累积肝脏的常染色体显性遗传多囊肾病-病例报道

2019-05-17

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

ARCH PATHOL LAB MED：染色体基因组阵列检测在未分类晚期肾细胞癌中的临床应用

2019-05-11

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

NAT GENET：人类结直肠癌类器官染色体不稳定性和核型进化过程

2019-05-04

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

BMC Med Genet：常染色体隐性非综合征听力损失患者中，MYO15A基因型表型相关性分析

2019-04-25

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

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

2019-03-07

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

AGING CELL：男性Y染色体年龄依赖性DNA甲基化模式

2019-03-02

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

RARS型骨髓增生异常综合征患者伴有ph染色体阳性1例

2019-02-22

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

病例分享 | 慢性髓系白血病双费城染色体阳性同时表达P210BCR-ABL1和P195BCR-ABL1

2019-02-18

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Haematologica：病例分享 | 慢性髓系白血病双费城染色体阳性同时表达P210BCR-ABL1和P195BCR-ABL1

2019-02-17

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Biochem Genet：新型常染色体隐性视网膜色素病变CNGA1基因突变（c.G622A）导致膜上CNGA1蛋白质减少

2019-02-02

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Bardoxolone治疗常染色体显性多囊肾病的III期试验正式开始

2019-01-30

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

INT J LAB HEMATOL：219例慢性髓系白血病合并染色体异常和/或酪氨酸激酶域突变的结果

2019-01-29

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

NATURE：自噬性细胞死亡保护染色体稳定性

2019-01-28

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Nat Commun：是男，是女，可不是XY染色体说了算这么简单……

2018-12-20

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Eur Urol：Y染色体上LncRNA对前列腺癌的促进作用机制获进展

2018-12-18

新生儿张玉军 (审核中...)

前往app查看评论内容

#染色体#

Eur J Med Genet：非综合征常染色体隐性听力损失的一个稀有变异-LHFPL5变异分析

2018-12-05

科室
- - 订阅+
  - 更多科室
工具
服务