Molecular Genetics and Complex Inheritance of Congenital Heart Disease

Congenital heart disease (CHD) is the most common congenital malformation and the leading cause of mortality therein. Genetic etiologies contribute to an estimated 90% of CHD cases, but so far, a molecular diagnosis remains unsolved in up to 55% of patients. Copy number variations and aneuploidy acc...

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Detalles Bibliográficos
Autores principales: Diab, Nicholas S., Barish, Syndi, Dong, Weilai, Zhao, Shujuan, Allington, Garrett, Yu, Xiaobing, Kahle, Kristopher T., Brueckner, Martina, Jin, Sheng Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307500/
https://www.ncbi.nlm.nih.gov/pubmed/34209044
http://dx.doi.org/10.3390/genes12071020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307500/
https://www.ncbi.nlm.nih.gov/pubmed/34209044
http://dx.doi.org/10.3390/genes12071020

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