Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500K SNP array genomic hybridization.
Friedman JM, Adam S, Arbour L, Armstrong L, Baross A, Birch P, Boerkoel C, Chan S, Chai D, Delaney AD, Flibotte S, Gibson WT, Langlois S, Lemyre E, Li HI, Macleod P, Mathers J, Michaud JL, McGillivray BC, Patel MS, Qian H, Rouleau GA, Van Allen MI, Yong SL, Zahir FR, Eydoux P, Marra MA.
BMC Genomics. 2009 Nov 16;10(1):526. [Epub ahead of print]PMID: 19917086 [PubMed - as supplied by publisher]Related articlesFree article