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/vufind/Search/Results?lookfor=%22Jin%2C+Yanhui%22&type=Person&sort=year
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PubPharm (81)
1
Analysis of three Chinese pedigrees affected with Hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2024
von
Ye, L.
|
Chen, H.
|
Su, Z.
| +5
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2
Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events
enthalten in:
International journal of laboratory hematology
| 2024
von
Chen, Y.
|
Qin, L.
|
Jin, Y.
| +4
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3
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency
enthalten in:
Annals of hematology
| 2024
von
Xu, F.
|
Zhou, X.
|
Jin, Y.
| +4
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4
Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency
enthalten in:
Annals of hematology
| 2024
von
Xu, F.
|
Zhang, K.
|
Xu, Q.
| +5
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5
Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*)
enthalten in:
Blood cells, molecules & diseases
| 2024
von
Zhang, K.
|
Ye, L.
|
Jin, Y.
| +5
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6
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency
enthalten in:
Annals of hematology
| 2024
von
Xu, F.
|
Zhou, X.
|
Jin, Y.
| +4
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7
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations
enthalten in:
Hamostaseologie
| 2023
von
Chen, Y.
|
Zhang, K.
|
Jin, Y.
| +4
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8
Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency
enthalten in:
Hamostaseologie
| 2023
von
Zhang, K.
|
Ye, L.
|
Jin, Y.
| +5
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9
Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅺ deficiency due to variant of F11 gene
enthalten in:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
| 2023
von
Wang, H.
|
Jiang, S.
|
Xia, H.
| +3
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10
Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency
enthalten in:
Annals of hematology
| 2023
von
Xu, F.
|
Zhang, K.
|
Xu, Q.
| +5
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Blood coagulation & fibrinolysis : an internati...
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Thema
59
Journal Article
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Case Reports
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9001-25-6
10
Factor VII
9
Gene mutation
9
Research Support, Non-U.S. Gov't
8
9001-30-3
8
English Abstract
8
Factor XII
8
Protein C
7
9001-32-5
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Fibrinogen
6
9013-55-2
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Factor XI
6
Genetic analysis
5
9001-24-5
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Factor V
4
CRM
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Expression study
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Factor XII deficiency
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Erscheinungszeitraum
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2020-
42
2010-2019
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23
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