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Yanhui Jin

Showing results (31-40 of 71) with videos related to

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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 1, 2024
[Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency]Bile Chen, Zuoting Xie, Zhou Zheng, et al.
Annals of Hematology|January 4, 2024
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiencyFei Xu, Xingxing Zhou, Yanhui Jin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 4, 2015
[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene]Yingyu Wang, Hongxiang Ding, Xiuping Hao, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 14, 2016
Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140sXiuping Hao, XiaoLi Cheng, Jiajia Ye, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[Genetic analysis and clinical features of a pedigree affected with hereditary coagulation factor Ⅶ deficiency caused by compound heterozygotic mutations]Yanhui Jin, Lihong Yang, Feng Zhang, et al.
Hamostaseologie|May 26, 2020
Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr)Siqi Liu, Shasha Luo, Lihong Yang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 26, 2025
[Analysis of a Chinese pedigree affected with hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene]Fei Xu, Anqing Zou, Haixiao Xie, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 4, 2026
Genotype-Phenotype Correlation of Hereditary Plasminogen Deficiency: Molecular Mechanisms From 18 Patients With Cerebral InfarctionYifan Lu, Haixiao Xie, Dandan Yu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 18, 2015
A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese familiesXiuping Hao, XiaoLi Cheng, Yingyu Wang, et al.
Hamostaseologie|June 15, 2023
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous MutationsYuan Chen, Ke Zhang, Yanhui Jin, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 1, 2024
[Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency]Bile Chen, Zuoting Xie, Zhou Zheng, et al.
Annals of Hematology|January 4, 2024
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiencyFei Xu, Xingxing Zhou, Yanhui Jin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 4, 2015
[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene]Yingyu Wang, Hongxiang Ding, Xiuping Hao, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 14, 2016
Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140sXiuping Hao, XiaoLi Cheng, Jiajia Ye, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 11, 2019
[Genetic analysis and clinical features of a pedigree affected with hereditary coagulation factor Ⅶ deficiency caused by compound heterozygotic mutations]Yanhui Jin, Lihong Yang, Feng Zhang, et al.
Hamostaseologie|May 26, 2020
Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr)Siqi Liu, Shasha Luo, Lihong Yang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 26, 2025
[Analysis of a Chinese pedigree affected with hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene]Fei Xu, Anqing Zou, Haixiao Xie, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 4, 2026
Genotype-Phenotype Correlation of Hereditary Plasminogen Deficiency: Molecular Mechanisms From 18 Patients With Cerebral InfarctionYifan Lu, Haixiao Xie, Dandan Yu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 18, 2015
A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese familiesXiuping Hao, XiaoLi Cheng, Yingyu Wang, et al.
Hamostaseologie|June 15, 2023
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous MutationsYuan Chen, Ke Zhang, Yanhui Jin, et al.
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