Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Kankan Su

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Clinical Laboratory|August 17, 2022
Pseudoleukocytopenia: a Case ReportXiang Qian, Kankan Su, Lixia Zhang
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 14, 2021
A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiencyKankan Su, Lin Wang, Mingshan Wang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 13, 2026
Genetic Analysis of a Family With Hereditary Factor V Deficiency Induced by Compound Heterozygous Variants (IVS24+3A>T and p.Asp2222Gly)Ben Huang, Yan Zhang, Litao Zhang, et al.
International Journal of Hematology|February 1, 2018
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriageAnqing Zou, Mingshan Wang, Yanhui Jin, 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.
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.
Hematology (Amsterdam, Netherlands)|February 16, 2017
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutationKankan Su, Yanhui Jin, Zhihai Miao, 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.
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.
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.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Clinical Laboratory|August 17, 2022
Pseudoleukocytopenia: a Case ReportXiang Qian, Kankan Su, Lixia Zhang
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 14, 2021
A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiencyKankan Su, Lin Wang, Mingshan Wang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 13, 2026
Genetic Analysis of a Family With Hereditary Factor V Deficiency Induced by Compound Heterozygous Variants (IVS24+3A>T and p.Asp2222Gly)Ben Huang, Yan Zhang, Litao Zhang, et al.
International Journal of Hematology|February 1, 2018
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriageAnqing Zou, Mingshan Wang, Yanhui Jin, 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.
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.
Hematology (Amsterdam, Netherlands)|February 16, 2017
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutationKankan Su, Yanhui Jin, Zhihai Miao, 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.
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.
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.
Pageof 2