The clinical application of array CGH for the detection of chromosomal defects in 20,126 unselected newborns

BACKGROUND: Array comparative genomic hybridization (CGH) is a powerful tool for detecting unbalanced chromosomal alterations. To validate the usefulness of array CGH in newborn screening, we examined 20,126 unselected infants. In addition, the number of newborns analyzed with array CGH is the large...

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Detalles Bibliográficos
Autores principales: Park, Sang-Jin, Jung, Eun Hye, Ryu, Ran-Suk, Kang, Hyun Woong, Chung, He Doo, Kang, Ho-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682880/
https://www.ncbi.nlm.nih.gov/pubmed/23725218
http://dx.doi.org/10.1186/1755-8166-6-21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682880/
https://www.ncbi.nlm.nih.gov/pubmed/23725218
http://dx.doi.org/10.1186/1755-8166-6-21

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