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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Detalles Bibliográficos
Autores principales: Hinton, Robert B., McBride, Kim L., Bleyl, Steven B., Bowles, Neil E., Border, William L., Garg, Vidu, Smolarek, Teresa A., Lalani, Seema R., Ware, Stephanie M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753096/
https://www.ncbi.nlm.nih.gov/pubmed/29371513
http://dx.doi.org/10.3390/jcdd2020076

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5753096/
https://www.ncbi.nlm.nih.gov/pubmed/29371513
http://dx.doi.org/10.3390/jcdd2020076

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