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...

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Bibliografiska uppgifter
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: S. Karger AG 2009
Ämnen:
Copy Number Variation and Inherited Disease
Länkar: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
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