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Yanhui Jin

Showing results (41-50 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|June 4, 2015
[Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency]Lihong Yang, Xiuping Hao, Yingyu Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 1, 2026
[Genetic analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅴ deficiency due to compound heterozygous variants IVS24+3A>T and p.Asp2222Gly]Langyi Qin, Shuangnyu Lin, Yaosheng Xie, et al.
Acta Haematologica|March 23, 2016
Identification of Genetic Defects Underlying FXII Deficiency in Four Unrelated Chinese PatientsLihong Yang, Yingyu Wang, Jianpin Zhou, et al.
Blood Cells, Molecules & Diseases|August 28, 2023
Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*)Ke Zhang, Longying Ye, Yanhui Jin, et al.
Hematology (Amsterdam, Netherlands)|April 2, 2019
Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiencyHaiyue Zhang, Siqi Liu, Chanchan Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 6, 2019
[Identification of compound heterozygous mutations of F11 gene in a pedigree affected with heriditary coagulation factor XI deficiency]Meina Liu, Xiaolong Li, Xingxing Zhou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 31, 2020
[Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene]Meina Liu, Yanhui Jin, Lihong Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 2019
Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121ArgHaiyue Zhang, Shasha Luo, Weiwei Fang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 25, 2020
Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutationsShasha Luo, Siqi Liu, Mengjie Xu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 3, 2019
A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patientSiqi Liu, Shasha Luo, Lihong Yang, et al.
Pageof 8

Showing results (41-50 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|June 4, 2015
[Identification of a novel heterozygous mutation in a pedigree with hereditary coagulation factor XII deficiency]Lihong Yang, Xiuping Hao, Yingyu Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 1, 2026
[Genetic analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅴ deficiency due to compound heterozygous variants IVS24+3A>T and p.Asp2222Gly]Langyi Qin, Shuangnyu Lin, Yaosheng Xie, et al.
Acta Haematologica|March 23, 2016
Identification of Genetic Defects Underlying FXII Deficiency in Four Unrelated Chinese PatientsLihong Yang, Yingyu Wang, Jianpin Zhou, et al.
Blood Cells, Molecules & Diseases|August 28, 2023
Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*)Ke Zhang, Longying Ye, Yanhui Jin, et al.
Hematology (Amsterdam, Netherlands)|April 2, 2019
Compound heterozygous mutations Glu502Lys and Met527Thr of the FXII gene in a patient with factor XII deficiencyHaiyue Zhang, Siqi Liu, Chanchan Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 6, 2019
[Identification of compound heterozygous mutations of F11 gene in a pedigree affected with heriditary coagulation factor XI deficiency]Meina Liu, Xiaolong Li, Xingxing Zhou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 31, 2020
[Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene]Meina Liu, Yanhui Jin, Lihong Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 2, 2019
Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121ArgHaiyue Zhang, Shasha Luo, Weiwei Fang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 25, 2020
Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutationsShasha Luo, Siqi Liu, Mengjie Xu, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 3, 2019
A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patientSiqi Liu, Shasha Luo, Lihong Yang, et al.
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