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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 18, 2022
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency
Haixiao Xie, Mingshan Wang, Yanhui Jin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
November 20, 2021
Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency
Huanhuan Wang, Shuting Jiang, Haixiao Xie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 26, 2025
[Genetic analysis of a family with inheritary coagulation factor Ⅹ deficiency due to compound heterozygous variants p.Phe71Ser and p.Val424Phe]
Shuangnyu Lin, Bile Chen, Zuoting Xie, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
March 16, 2013
A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family
Liqing Zhu, Mingshan Wang, Haixiao Xie, et al.
Hematology (Amsterdam, Netherlands)
|
December 24, 2016
Genetic analysis of a hereditary factor XII deficiency pedigree of a consanguineous marriage due to a homozygous F12 gene mutation: Gly341Arg
Xiaoli Cheng, Lihong Yang, Guoyong Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 14, 2018
[Phenotypic and mutational analysis of a pedigree affected with hereditary coagulation factor Ⅴ deficiency]
Mengcha Tian, Hong Xia, Zhishan Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 10, 2016
[Phenotypic and genetic analysis of two pedigrees affected with hereditary antithrombin deficiency]
Xiuping Hao, Yanhui Jin, Xiaoli Cheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
February 11, 2017
[Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency]
Lihong Yang, Yanhui Jin, Ting Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 11, 2014
Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia
Yingyu Wang, Liqing Zhu, Xiuping Hao, et al.
Acta Haematologica
|
July 19, 2021
Significance of the p.Phe218Ser and p.Gly304Glu F5 Variants in Hereditary Factor V Deficiency
Rujiao Dong, Guoliang Chen, Yanhui Jin, et al.
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of 8
Search research articles
Search
Showing results (11-20 of 71) with videos related to
Sort By:
Page
of 8
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
August 18, 2022
A novel F13A1 gene mutation (Arg208Pro) in a Chinese patient with factor XIII deficiency
Haixiao Xie, Mingshan Wang, Yanhui Jin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
November 20, 2021
Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency
Huanhuan Wang, Shuting Jiang, Haixiao Xie, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 26, 2025
[Genetic analysis of a family with inheritary coagulation factor Ⅹ deficiency due to compound heterozygous variants p.Phe71Ser and p.Val424Phe]
Shuangnyu Lin, Bile Chen, Zuoting Xie, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
March 16, 2013
A novel fibrinogen mutation (γ Thr277Arg) causes hereditary hypofibrinogenemia in a Chinese family
Liqing Zhu, Mingshan Wang, Haixiao Xie, et al.
Hematology (Amsterdam, Netherlands)
|
December 24, 2016
Genetic analysis of a hereditary factor XII deficiency pedigree of a consanguineous marriage due to a homozygous F12 gene mutation: Gly341Arg
Xiaoli Cheng, Lihong Yang, Guoyong Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 14, 2018
[Phenotypic and mutational analysis of a pedigree affected with hereditary coagulation factor Ⅴ deficiency]
Mengcha Tian, Hong Xia, Zhishan Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
April 10, 2016
[Phenotypic and genetic analysis of two pedigrees affected with hereditary antithrombin deficiency]
Xiuping Hao, Yanhui Jin, Xiaoli Cheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
February 11, 2017
[Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency]
Lihong Yang, Yanhui Jin, Ting Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 11, 2014
Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia
Yingyu Wang, Liqing Zhu, Xiuping Hao, et al.
Acta Haematologica
|
July 19, 2021
Significance of the p.Phe218Ser and p.Gly304Glu F5 Variants in Hereditary Factor V Deficiency
Rujiao Dong, Guoliang Chen, Yanhui Jin, et al.
Page
of 8