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...
Saved in:
| 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: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Identification of Novel Gene Variants for Autism Spectrum Disorders in the Lebanese Population Using Whole-Exome Sequencing
by: Perla Gerges (18394857)
Published: (2022) -
Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
by: Athar Khalil (5906330)
Published: (2020) -
Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review
by: Amal Elfatih (14778550)
Published: (2021) -
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants
by: Ana Rio-Machin (19686124)
Published: (2020) -
The Role of Cilia and the Complex Genetics of Congenital Heart Disease
by: George C. Gabriel (11469982)
Published: (2024)