Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis

OBJECTIVES: Our aim was to determine the frequency of genomic imbalances in neonates with birth defects by using targeted array-based comparative genomic hybridization, also known as chromosomal microarray analysis. METHODS: Between March 2006 and September 2007, 638 neonates with various birth defe...

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Bibliografiset tiedot
Päätekijät: Lu, Xin-Yan, Phung, Mai T., Shaw, Chad A., Pham, Kim, Neil, Sarah E., Patel, Ankita, Sahoo, Trilochan, Bacino, Carlos A., Stankiewicz, Pawel, Lee Kang, Sung-Hae, Lalani, Seema, Chinault, A. Craig, Lupski, James R., Cheung, Sau W., Beaudet, Arthur L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2008
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2795566/
https://ncbi.nlm.nih.gov/pubmed/19047251
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.2008-0297
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