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[会议论文] 作者：Qian Liang,Mingjie Xiang,Yeling Lu,Qiulan Ding,Xuefeng Wang,Xiaodong Xi,Hongli Wang,
来源：中华医学会第八次全国中青年检验医学学术会议 年份：2014
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[会议论文] 作者：Xi Wu,Guoling You,Xiaodong Xi,Hongli Wang,Yeling Lu,Qiulan Ding,Jing Dai,Xuefeng Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
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Identification and characterization of a novel aberrant pattern of intron 1 inversion with concomita
[会议论文] 作者：Guoling You,Kun Chi,Xiaodong Xi,Hongli Wang,Yeling Lu,Qiulan Ding,Jing Dai,Xuefeng Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
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Identification and characterization of a novel aberrant pattern of intron 1 inversion with concomita
[会议论文] 作者：Guoling You,Kun Chi,Yeling Lu,Qiulan Ding,Jing Dai,Xiaodong Xi,Hongli Wang,Xuefeng Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
Aims Intron 1 inversion (Inv1) is a recurrent causative mutation of haemophilia A (HA) and is responsible for 1-5 ％of severe HA.Inv1 occurs as a result of intrachromosomal homologous recombination bet...
[会议论文] 作者：Xi Wu,Yeling Lu,Qiulan Ding,Guoling You,Jing Dai,Xiaodong Xi,Hongli Wang,Xuefeng Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
Objective Large deletions in the F9 gene are detected in approximately 5 ％of patients with severe haemophilia B,but only a few deletion breakpoints have been characterized precisely until now....
[会议论文] 作者：Qian Liang,Mingjie Xiang,Yeling Lu,Yufeng Ruan,Qiulan Ding,Xuefeng Wang,Xiaodong Xi,Hongli Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
Objective Mutations affecting splice site comprise approximately 7.5 ％of the known F8 gene mutations but only a few were verified at mRNA level.In present study,we characterized the pathogenic effects...
Original Article Clinical features and molecular basis of 102 Chinese patients with congenital dysfi
[会议论文] 作者：Jingyi Zhou,Qiulan Ding,Yaopeng Chen,Qi Ouyang,Linlin Jiang,Jing Dai,Yeling Lu,Xi Wu,Qian Liang,Hongli,
来源：第十届全国检验与临床学术会议暨2015年中国医师协会检验医师年会 年份：2015
Introduction: Congenital dysfibrinogenemia(CD)is a rare qualitative disorder of fibrinogen(Fg)with heterogeneous clinical manifestations....
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