Hongxiang Ding

Wenzhou, China

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications

Analysis of cerebral infarction caused by dysplasminogenemia in three pedigrees.

Analysis of cerebral infarction caused by dysplasminogenemia in three pedigrees.

Journal: Frontiers in genetics
Published: January 22, 2023

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 03, 2021

Analysis of Phenotype and Genotypein an Inherited Coagulation Factor VII Deficiency Pedigree.

Analysis of Phenotype and Genotypein an Inherited Coagulation Factor VII Deficiency Pedigree.

Journal: Clinical laboratory
Published: December 19, 2019

Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene

Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 09, 2019

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.

Journal: Human mutation
Published: March 03, 2019

A case of a severe factor XI deficiency in a Chinese woman with heavy menorrhagia.

A case of a severe factor XI deficiency in a Chinese woman with heavy menorrhagia.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: February 06, 2019

Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide.

Diagnostic Error of a Patient with Combined Inherited Factor VII and Factor X Deficiency due to Accidental Ingestion of a Diphacinone Rodenticide.

Journal: Clinical laboratory
Published: February 07, 2017

Molecular Characterization of a Novel Missense Mutation (Asp538Asn) in a Chinese Patient with Factor XII Deficiency.

Molecular Characterization of a Novel Missense Mutation (Asp538Asn) in a Chinese Patient with Factor XII Deficiency.

Journal: Clinical laboratory
Published: February 18, 2016

Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency

Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 15, 2015

Congenital hypofibrinogenemia associated with a novel mutation in FGG gene

Congenital hypofibrinogenemia associated with a novel mutation in FGG gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 04, 2015

Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families.

Novel mutations (γTrp208Leu and γLys232Thr) leading to congenital hypofibrinogenemia in two unrelated Chinese families.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: June 11, 2014
Showing 1-11 of 11

Last Updated: 09/26/2026