Benign copy number changes in clinical cytogenetic diagnostics by array CGH

A database of apparently benign copy number variants (bCNVs) detected by a Spectral Genomics Inc./PerkinElmer BAC array platform has been maintained through the University of Utah Comparative Genomic Hybridization laboratory since 2005. The target population for this database represents 1,275 patien...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Whitby, H., Tsalenko, A., Aston, E., Tsang, P., Mitchell, S., Bayrak-Toydemir, P., Hopkins, C., Peters, G., Bailey, D.K., Bruhn, L., Brothman, A.R.
Format: Artigo
Sprog:Inglês
Udgivet: S. Karger AG 2009
Fag:
Copy Number Variation and Inherited Disease
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2920185/
https://ncbi.nlm.nih.gov/pubmed/19287143
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000184696
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker