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...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: S. Karger AG 2009
Onderwerpen:
Copy Number Variation and Inherited Disease
Online toegang: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: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items