Xiaoli G. Cheng
State Key Laboratory Of Oral & Maxillofacial Reconstruction And Regeneration, Shaanxi Key Laboratory Of Stomatology
Xi'an, 710032, China
Xi'an, 710032, China
Last Updated: 09/26/2026
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Found 21 publications
Analysis of a Chinese pedigree affected with Hereditary factor Ⅴ deficiency due to compound heterozygous variants of F5 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 06, 2026
Research and progress in etiology, prevention and treatment strategies of secondary caries
Journal: Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology
Published: January 03, 2024
Analysis of a Chinese pedigree affected with Hereditary coagulation factor Ⅻ deficiency due to compound heterozygous variants of F12 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 23, 2023
Detection and Gene Mutation Analysis of Three Variations in Two Unrelated Chinese Hereditary Coagulation Factor XI Deficiency Families.
Journal: Acta haematologica
Published: November 13, 2021
PARP1 rs1136410 Val762Ala contributes to an increased risk of overall cancer in the East Asian population: a meta-analysis.
Journal: The Journal of international medical research
Published: March 12, 2021
Analysis of a pedigree affected with hereditary coagulation factor XII deficiency due to a homozygous 252delAsn deletion of F12 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 04, 2020
Significance of the p.Phe218Ser and p.Gly304Glu F5 Variants in Hereditary Factor V Deficiency.
Journal: Acta haematologica
Published: January 14, 2020
Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 14, 2018
Analysis of a consanguineous pedigree affected with hereditary coagulation factor XII deficiency caused by homozygous Gly341Arg mutation
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 09, 2018
A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: December 19, 2017
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage.
Journal: International journal of hematology
Published: May 12, 2017
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.
Journal: Hematology (Amsterdam, Netherlands)
Published: February 16, 2017
Last Updated: 09/26/2026