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Last Updated: 10/31/2025
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Found 542 publications
Prolonged Asymptomatic Activated Partial Thromboplastin Time: Incidental Finding of Factor XII Deficiency: A Coagulation Conundrum in the Operating Room During an Emergency Coronary Artery Bypass Surgery.
Journal: Journal of cardiothoracic and vascular anesthesia
Published: August 16, 2025
Genetic analysis for an inherited coagulation factor XII deficiency pedigree.
Journal: Hematology (Amsterdam, Netherlands)
Published: July 02, 2025
Managing Placenta Accreta Spectrum: Diagnosis, Surgical Strategies, and Postoperative Care.
Journal: Cureus
Published: June 16, 2025
Analysis of a Chinese pedigree with Hereditary coagulation factor Ⅻ deficiency due to compound heterozygous variants of Ⅻ gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 15, 2025
A novel homozygous frameshift mutation (p.Lys365Glnfs*69) in a family with hereditary factor XII deficiency: a case report.
Journal: Journal of hematopathology
Published: March 19, 2025
Coagulation factor XII haploinsufficiency is protective against venous thromboembolism in a population-scale multidimensional analysis.
Journal: Nature communications
Published: February 19, 2025
Case Report: Two children with factor XII deficiency caused by novel F12 compound heterozygous variants.
Journal: Frontiers in pediatrics
Published: January 04, 2025
Impact of heparin-aspirin therapy in patients with recurrent pregnancy loss characterized by thrombophilia resistant to low-dose aspirin therapy: A retrospective study.
Journal: Reproductive medicine and biology
Published: September 10, 2024
Genetic analysis of a pedigree with hereditary coagulation factor XII deficiency.
Journal: Annals of hematology
Published: August 26, 2024
Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene
Journal: Zhongguo shi yan xue ye xue za zhi
Published: June 27, 2024
Clinical and genetic spectrum of factor XII deficiency in the Han population of East China.
Journal: Orphanet journal of rare diseases
Published: May 12, 2024
Last Updated: 10/31/2025