Tromboembolia pulmonar en un paciente con trombofilia familiar de origen genético debida a homocigosis en mutación 20209C>T
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference8 articles.
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2. Abnormal melt curve profile during prothrombin 20210G --> A analysis due to the 20209C --> T variant;Dunn;Blood Coagul Fibrinolysis,2006
3. The prothrombin 20209C>T sequence variant: To test or not to test;Quigley;J Assoc Genet Technol,2007
4. Prothrombin 20209C>T: 16 new cases, association with the 19911A>G polymorphism, and literature review;Warshawsky;J Thromb Haemost,2009
5. Prothrombin gene variants in non-Caucasians with fetal loss and intrauterine growth retardation;Schrijver;J Mol Diagn,2003
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1. A Rare Prothrombin Gene Mutation C20209T in a South African Patient with Pulmonary Embolism in Pregnancy: a Case Study and Systematic Review;Clinical Laboratory;2019
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