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Article

Determining genetic variants in children and adolescents suffering from tetralogy of Fallot with a positive family history: methodology.

Acta bio-medica : Atenei Parmensis - 26 Jun 2020

Sabri Mohammad Reza, Gharipour Mojgan, Tayebi Naeimeh, Sadeghian Ladan, Javanmard Shaghayegh Haghjooy, Sarrafzadegan Nizal

Abstract excerpt

BACKGROUND AND AIM: Congenital heart disease (CHD) affects near 1% of all live births and is considered to be the main reason of morbidity and mortality in early childhood. In this study, we investigated molecular genetics factors associated with Tetralogy of Fallot (TOF) using high throughput technologies in the consanguineous families with at least 2 affected individual. METHOD: This family study started in...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33525261
DOI: 10.23750/abm.v91i4.8410
PMCID: PMC7927530

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