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From microscopes to microarrays: dissecting recurrent chromosomal rearrangements

Submicroscopic chromosomal rearrangements that lead to copy-number changes have been shown to underlie distinctive and recognizable clinical phenotypes. The sensitivity to detect copy-number variation has escalated with the advent of array comparative genomic hybridization (CGH), including BAC and o...

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Detalles Bibliográficos
Main Authors: Emanuel, Beverly S., Saitta, Sulagna C.
Formato: Artigo
Idioma:Inglês
Publicado: 2007
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2858421/
https://ncbi.nlm.nih.gov/pubmed/17943194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrg2136
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