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Yanhui Jin

Showing results (21-30 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|October 31, 2023
[Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅺ deficiency due to variant of F11 gene]Huanhuan Wang, Suting Jiang, Huinan Xia, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 30, 2013
Double heterozygous mutations Gln100Leu and His348Gln of the F7 gene in a patient with factor VII deficiencyMin Li, Fangxiu Zheng, Yanhui Jin, et al.
Hematology (Amsterdam, Netherlands)|December 15, 2020
A novel homozygous missense mutation (Met527Ile) in a consanguineous marriage family with inherited factor XII deficiencyMeina Liu, Huanhuan Wang, Miaomiao Lin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 15, 2018
A novel mutation (Tyr503Cys) in a severe factor XI deficiencyKankan Su, Xiaoxiao Cai, Wenli Xia, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 16, 2020
Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese familySiqi Liu, Huanhuan Wang, Qiyu Xu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2018
[Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation]Lihong Yang, Saiyan Jin, Weidan Ji, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 8, 2013
[Identification of a novel mutation of factor XII gene in a family with coagulation FXII deficiency]Haixiao Xie, Meiyan Lv, Xiaoli Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 16, 2018
Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosisKankan Su, Haiyue Zhang, Weiwei Fang, et al.
Placenta|June 14, 2025
Insufficient expression of VTN promotes the development of early-onset severe preeclampsia through the HEY1/autophagy signaling pathwayGonghua Qi, Yanmin Gong, Yi Li, et al.
Cell Death Discovery|March 2, 2025
Insufficient expression of COL6A1 promotes the development of early-onset severe preeclampsia by inhibiting the APJ/AKT signaling pathwayGonghua Qi, Yanmin Gong, Yi Li, et al.
Pageof 8

Showing results (21-30 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|October 31, 2023
[Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅺ deficiency due to variant of F11 gene]Huanhuan Wang, Suting Jiang, Huinan Xia, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 30, 2013
Double heterozygous mutations Gln100Leu and His348Gln of the F7 gene in a patient with factor VII deficiencyMin Li, Fangxiu Zheng, Yanhui Jin, et al.
Hematology (Amsterdam, Netherlands)|December 15, 2020
A novel homozygous missense mutation (Met527Ile) in a consanguineous marriage family with inherited factor XII deficiencyMeina Liu, Huanhuan Wang, Miaomiao Lin, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|March 15, 2018
A novel mutation (Tyr503Cys) in a severe factor XI deficiencyKankan Su, Xiaoxiao Cai, Wenli Xia, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 16, 2020
Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese familySiqi Liu, Huanhuan Wang, Qiyu Xu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2018
[Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation]Lihong Yang, Saiyan Jin, Weidan Ji, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 8, 2013
[Identification of a novel mutation of factor XII gene in a family with coagulation FXII deficiency]Haixiao Xie, Meiyan Lv, Xiaoli Yang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 16, 2018
Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosisKankan Su, Haiyue Zhang, Weiwei Fang, et al.
Placenta|June 14, 2025
Insufficient expression of VTN promotes the development of early-onset severe preeclampsia through the HEY1/autophagy signaling pathwayGonghua Qi, Yanmin Gong, Yi Li, et al.
Cell Death Discovery|March 2, 2025
Insufficient expression of COL6A1 promotes the development of early-onset severe preeclampsia by inhibiting the APJ/AKT signaling pathwayGonghua Qi, Yanmin Gong, Yi Li, et al.
Pageof 8