Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

While numerous studies have implicated copy number variants (CNVs) in a range of neurological phenotypes, the impact relative to disease severity has been difficult to ascertain due to small sample sizes, lack of phenotypic details, and heterogeneity in platforms used for discovery. Using a customiz...

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Detalles Bibliográficos
Autores principales: Girirajan, Santhosh, Brkanac, Zoran, Coe, Bradley P., Baker, Carl, Vives, Laura, Vu, Tiffany H., Shafer, Neil, Bernier, Raphael, Ferrero, Giovanni B., Silengo, Margherita, Warren, Stephen T., Moreno, Carlos S., Fichera, Marco, Romano, Corrado, Raskind, Wendy H., Eichler, Evan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213131/
https://www.ncbi.nlm.nih.gov/pubmed/22102821
http://dx.doi.org/10.1371/journal.pgen.1002334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213131/
https://www.ncbi.nlm.nih.gov/pubmed/22102821
http://dx.doi.org/10.1371/journal.pgen.1002334

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