Integrated small copy number variations and epigenome maps of disorders of sex development

Small copy number variations (CNVs) have typically not been analyzed or reported in clinical settings and hence have remained underrepresented in databases and the literature. Here, we focused our investigations on these small CNVs using chromosome microarray analysis (CMA) data previously obtained...

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Detalles Bibliográficos
Autores principales: Amarillo, Ina E, Nievera, Isabelle, Hagan, Andrew, Huchthagowder, Vishwa, Heeley, Jennifer, Hollander, Abby, Koenig, Joel, Austin, Paul, Wang, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899613/
https://www.ncbi.nlm.nih.gov/pubmed/27340555
http://dx.doi.org/10.1038/hgv.2016.12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899613/
https://www.ncbi.nlm.nih.gov/pubmed/27340555
http://dx.doi.org/10.1038/hgv.2016.12

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