A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

BACKGROUND: Chromosomal microarray analysis (CMA) provides an opportunity to understand genetic causes of congenital heart disease (CHD). The methods for describing cardiac phenotypes in patients with CMA abnormalities have been inconsistent, which may complicate clinical interpretation of abnormal...

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Detalles Bibliográficos
Autores principales: Landis, Benjamin J., Helvaty, Lindsey R., Geddes, Gabrielle C., Lin, Jiuann‐Huey Ivy, Yatsenko, Svetlana A., Lo, Cecilia W., Border, William L., Wechsler, Stephanie Burns, Murali, Chaya N., Azamian, Mahshid S., Lalani, Seema R., Hinton, Robert B., Garg, Vidu, McBride, Kim L., Hodge, Jennelle C., Ware, Stephanie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547279/
https://www.ncbi.nlm.nih.gov/pubmed/37681527
http://dx.doi.org/10.1161/JAHA.123.029340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547279/
https://www.ncbi.nlm.nih.gov/pubmed/37681527
http://dx.doi.org/10.1161/JAHA.123.029340

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