Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry

Investigation of Genetic Causes in Patients with Congenital Heart Disease in Qatar: Findings from the Sidra Cardiac Registry

<div><p>Congenital heart disease (CHD) is one of the most common forms of birth defects worldwide, with a prevalence of 1–2% in newborns. CHD is a multifactorial disease partially caused by genetic defects, including chromosomal abnormalities and single gene mutations. Here, we describe...

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Bibliographic Details
Main Author: Sarah Okashah (18282262) (author)
Other Authors: Dhanya Vasudeva (18002494) (author), Aya El Jerbi (18282265) (author), Houssein Khodjet-El-khil (18282268) (author), Mashael Al-Shafai (3466301) (author), Najeeb Syed (12561967) (author), Marios Kambouris (3441308) (author), Sharda Udassi (18282271) (author), Luis R. Saraiva (18282274) (author), Hesham Al-Saloos (18282277) (author), Jai Udassi (18282280) (author), Kholoud N. Al-Shafai (18282283) (author)
Published: 2022
Subjects:
Biological sciences
Genetics
congenital heart defect
Qatar
genetic investigation
whole exome sequencing
single-nucleotide variant
chromosomal abnormalities
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