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

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 the Sidra Cardiac Re...

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Detalles Bibliográficos
Autores principales: Okashah, Sarah, Vasudeva, Dhanya, El Jerbi, Aya, Khodjet-El-khil, Houssein, Al-Shafai, Mashael, Syed, Najeeb, Kambouris, Marios, Udassi, Sharda, Saraiva, Luis R., Al-Saloos, Hesham, Udassi, Jai, Al-Shafai, Kholoud N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407366/
https://www.ncbi.nlm.nih.gov/pubmed/36011280
http://dx.doi.org/10.3390/genes13081369

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407366/
https://www.ncbi.nlm.nih.gov/pubmed/36011280
http://dx.doi.org/10.3390/genes13081369

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