De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature

BACKGROUND: Human height is a complex trait with a strong genetic basis. Recently, a significant association between rare copy number variations (CNVs) and short stature has been identified, and candidate genes in these rare CNVs are being explored. This study aims to evaluate the association betwee...

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Detalles Bibliográficos
Autores principales: Yu, Yongguo, Yao, RuEn, Wang, Lili, Fan, Yanjie, Huang, Xiaodong, Hirschhorn, Joel, Dauber, Andrew, Shen, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574214/
https://www.ncbi.nlm.nih.gov/pubmed/26376624
http://dx.doi.org/10.1186/s12864-015-1898-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4574214/
https://www.ncbi.nlm.nih.gov/pubmed/26376624
http://dx.doi.org/10.1186/s12864-015-1898-1

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