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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Detalhes bibliográficos
Publicado no:Hum Genome Var
Main Authors: Amarillo, Ina E, Nievera, Isabelle, Hagan, Andrew, Huchthagowder, Vishwa, Heeley, Jennifer, Hollander, Abby, Koenig, Joel, Austin, Paul, Wang, Ting
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4899613/
https://ncbi.nlm.nih.gov/pubmed/27340555
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2016.12
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