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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Detalhes bibliográficos
Publicado no:J Cardiovasc Dev Dis
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: MDPI 2015
Assuntos:
Communication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5753096/
https://ncbi.nlm.nih.gov/pubmed/29371513
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcdd2020076
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