22Q11 DELETION AND POLYMORPHISMS ASSOCIATED WITH COAGULOPATHY IN TETRALOGY OF FALLOT PATIENT: CASE REPORT

22Q11 DELETION AND POLYMORPHISMS ASSOCIATED WITH COAGULOPATHY IN TETRALOGY OF FALLOT PATIENT: CASE REPORT

Background: In recent years, there has been a notable effort to investigate the genetic mechanisms contributing to the development of congenital heart diseases (CHD) and their various forms of presentation. Aim: This study aims to examine and characterize the presence of multiple genetic alterations...

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Bibliographic Details
Main Authors: EJS Freitas, AGS Gbadamassi, MMP Luciano, JNV Silva, IPC Tavares, ACS Castro, MOO Nascimento, RMM Iimori, MS Gonçalves, JPM Neto
Format: Article
Language:English
Published: Elsevier 2023-10-01
Series:Hematology, Transfusion and Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S2531137923019740

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http://www.sciencedirect.com/science/article/pii/S2531137923019740

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