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[会议论文] 作者：Jingyi Zhou,Linlin Jiang,Qiulan Ding,Xuefeng Wang,Xiaodong Xi,Hongli Wang,
来源：中国医院协会临床检验管理专业委员会第七届全国临床检验实验室管理学术会议暨中华医学会第十次全国检验医学学术会议(2013N 年份：2013
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[会议论文] 作者：Jingyi Zhou,Linlin Jiang,Qiulan Ding,Xiaodong Xi,Xuefeng Wang,Hongli Wang,
来源：中国医院协会临床检验管理专业委员会第七届全国临床检验实验室管理学术会议暨中华医学会第十次全国检验医学学术会议(2013N 年份：2013
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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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Genetic analysis of inherited fibrinogen disorders in 43 patients and application of thrombelastogra
[会议论文] 作者：Jingyi Zhou,Linlin Jiang,Qi Ouyang,Xiaodong Xi,Hongli Wang,Qiulan Ding,Xuefeng Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
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Genetic analysis of inherited fibrinogen disorders in 43 patients and application of thrombelastogra
[会议论文] 作者：Jingyi Zhou,Qiulan Ding,Linlin Jiang,Qi Ouyang,Xuefeng Wang,Xiaodong Xi,Hongli Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
Background Hereditary fibrinogen disorders include quantitative abnormality (afibrinogenemia and hypofibrinogenemia),qualitative abnormality (dysfibrinogenemia) or both (hypo-dysfibrinogenemia).Inheri...
[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...
Genotypes of F9 gene and polymorphisms in immune response genes associated with inhibitor developmen
[会议论文] 作者：Jingyi Zhou,Qiulan Ding,Zhenping Chen,Hongbin Yang,Lin Lin,Hongli Wang,Xuefeng Wang,Runhui Wu,
来源：The 35th World Congress of the International Society of Hema 年份：2014
Background and Objectives The development of inhibitors is a severe complication of factor IX (FIX) substitution treatment for haemophilia B (HB).The aim of this study is to investigate the associatio...
[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：Yanyan Shao,Yanan Cao,Qiulan Ding,Yanling Lu,Jing Dai,Xiaodong Xi,Xuefeng Wang,Hongli Wang,
来源：The 35th World Congress of the International Society of Hema 年份：2014
Aims Factor XI deficiency is a mild bleeding tendency disorder with an autosomal heredity,occurring at a frequency of one in a million in the general population.This condition is more common among cer...
[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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