Publications by authors named "Manlin Zeng"

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Complications owing to oesophageal impaction of button batteries and risk factors in children in China: a review.
Manlin Zeng, Jing Huang, Lianming Liao, Ying Chen

Paediatr Int Child Health· September 2025

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Molecular mechanism analysis of a family with hereditary coagulation FXI deficiency caused by compound heterozygous mutations.
Yuan Chen, Manlin Zeng, Ke Zhang, Longying Ye, Shuting Jiang

Blood Coagul Fibrinolysis· December 2024

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Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.
Fei Xu, Ke Zhang, Qiyu Xu, Longying Ye, Manlin Zeng

Ann Hematol· February 2024

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Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations.
Yuan Chen, Ke Zhang, Yanhui Jin, Manlin Zeng, Kaiqi Jia

Hamostaseologie· December 2023

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A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia.
Kaiqi Jia, Manlin Zeng, Xiaoyong Zheng, Haixiao Xie, Lihong Yang

Hamostaseologie· December 2023

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Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency.
Ke Zhang, Longying Ye, Yanhui Jin, Yuan Chen, Manlin Zeng

Hamostaseologie· December 2023

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A novel mutation p.Met1Val in SERPINC1 gene causes hereditary antithrombin deficiency in a Chinese family with thrombotic disease.
Manlin Zeng, Kaiqi Jia, Meina Liu, Mingshan Wang, Lihong Yang

Thromb Res· December 2023

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Erratum: A Novel Fibrinogen Mutation p.BβAla68Asp Causes an Inherited Dysfibrinogenemia.
Kaiqi Jia, Manlin Zeng, Xiaoyong Zheng, Haixiao Xie, Lihong Yang

Hamostaseologie· December 2023

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Analysis of an Inherited FXII Deficiency Pedigree Associated with Double Heterozygous Mutations in the F12 Gene.
Manlin Zeng, Kaiqi Jia, Haixiao Xie, Yaosheng Xie, Lihong Yang

Indian J Hematol Blood Transfus· October 2023

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Gene Variants in Two Families with Inherited Coagulation Factor XI Deficiency and Identification of Mutations.
Shuting Jiang, Yuan Chen, Meina Liu, Manlin Zeng, Lihong Yang

Acta Haematol· March 2023

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[Genetic analysis of two Chinese pedigrees affected with Hereditary hypofibrinemia due to missense variants].
Xiaoyong Zheng, Yi Chen, Mengzhen Wen, Yanhui Jin, Manlin Zeng

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· March 2023

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