Deletion of a single-copy DAAM1 gene in congenital heart defect: a case report

BACKGROUND: With an increasing incidence of congenital heart defects (CHDs) in recent years, genotype-phenotype correlation and array-based methods have contributed to the genome-wide analysis and understanding of genetic variations in the CHD population. Here, we report a copy number deletion of ch...

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Detalles Bibliográficos
Autores principales: Bao, Bihui, Zhang, Liang, Hu, Hua, Yin, Shuxin, Liang, Zhiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482563/
https://www.ncbi.nlm.nih.gov/pubmed/22857009
http://dx.doi.org/10.1186/1471-2350-13-63

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3482563/
https://www.ncbi.nlm.nih.gov/pubmed/22857009
http://dx.doi.org/10.1186/1471-2350-13-63

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