SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

BACKGROUND: Heterotaxy-spectrum cardiovascular disorders are challenging for traditional genetic analyses because of clinical and genetic heterogeneity, variable expressivity, and non-penetrance. In this study, high-resolution SNP genotyping and exon-targeted array comparative genomic hybridization...

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Detalles Bibliográficos
Autores principales: Tariq, Muhammad, Belmont, John W, Lalani, Seema, Smolarek, Teresa, Ware, Stephanie M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308054/
https://www.ncbi.nlm.nih.gov/pubmed/21936905
http://dx.doi.org/10.1186/gb-2011-12-9-r91

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308054/
https://www.ncbi.nlm.nih.gov/pubmed/21936905
http://dx.doi.org/10.1186/gb-2011-12-9-r91

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