Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification

BACKGROUND: Connective tissue diseases characterized by aortic aneurysm, such as Marfan syndrome, Loeys-Dietz syndrome and Ehlers Danlos syndrome type IV are heterogeneous and despite overlapping phenotypes, the natural history, clinical manifestations and interventional course for each diagnosis ca...

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Detalles Bibliográficos
Autores principales: Furtado, Larissa V, Wooderchak-Donahue, Whitney, Rope, Alan F, Yetman, Angela T, Lewis, Tracey, Plant, Parker, Bayrak-Toydemir, Pinar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196690/
https://www.ncbi.nlm.nih.gov/pubmed/21936929
http://dx.doi.org/10.1186/1471-2350-12-119

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3196690/
https://www.ncbi.nlm.nih.gov/pubmed/21936929
http://dx.doi.org/10.1186/1471-2350-12-119

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