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 t...

Deskribapen osoa

Xehetasun bibliografikoak

Egile Nagusiak:	Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Wiley 2023-09-01
Saila:	Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Gaiak:	chromosomal microarray congenital heart disease conotruncal defects genomics neurodevelopment
Sarrera elektronikoa:	https://www.ahajournals.org/doi/10.1161/JAHA.123.029340
Etiketak:	Etiketa erantsi Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!