Observations on Copy Number Variations in a Kidney-yang Deficiency Syndrome Family

We have performed an analysis of a family with kidney-yang deficiency syndrome (KDS) in order to determine the structural genomic variations through a novel approach designated as “copy number variants” (CNVs). Twelve KDS subjects and three healthy spouses from this family were included in this stud...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Wei Wei, Gao, Yong Xiang, Zhou, Li Ping, Duan, Azure, Tan, Ling Ling, Li, Wan Zhen, Yan, Min, Yang, Hong Ya, Yan, Shi Lin, Wang, Mi Qu, Ding, Wei Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136678/
https://www.ncbi.nlm.nih.gov/pubmed/21811512
http://dx.doi.org/10.1093/ecam/neq069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136678/
https://www.ncbi.nlm.nih.gov/pubmed/21811512
http://dx.doi.org/10.1093/ecam/neq069

Ejemplares similares