Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

BACKGROUND: Array comparative genomic hybridization (CGH) is currently the most powerful method for detecting chromosomal alterations in pre and postnatal clinical cases. In this study, we developed a BAC based array CGH analysis platform for detecting whole genome DNA copy number changes including...

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Detalles Bibliográficos
Autores principales: Park, Sang-Jin, Jung, Eun Hye, Ryu, Ran-Suk, Kang, Hyun Woong, Ko, Jung-Min, Kim, Hyon J, Cheon, Chong Kun, Hwang, Sang-Hyun, Kang, Ho-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114015/
https://www.ncbi.nlm.nih.gov/pubmed/21549014
http://dx.doi.org/10.1186/1755-8166-4-12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3114015/
https://www.ncbi.nlm.nih.gov/pubmed/21549014
http://dx.doi.org/10.1186/1755-8166-4-12

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