Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

Cardiovascular malformations (CVMs) are the most common birth defect, occurring in 1%–5% of all live births. Although the genetic contribution to CVMs is well recognized, the genetic causes of human CVMs are identified infrequently. In addition, a failure of systematic deep phenotyping of CVMs, resu...

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Bibliographic Details
Main Authors: Robert B. Hinton, Kim L. McBride, Steven B. Bleyl, Neil E. Bowles, William L. Border, Vidu Garg, Teresa A. Smolarek, Seema R. Lalani, Stephanie M. Ware
Format: Article
Language:English
Published: MDPI AG 2015-04-01
Series:Journal of Cardiovascular Development and Disease
Subjects:
genetics
genomics
pediatrics
cardiovascular malformation
registry
chromosome microarray
copy number variation
Online Access:http://www.mdpi.com/2308-3425/2/2/76

Internet

http://www.mdpi.com/2308-3425/2/2/76

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