A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s12041-014-0369-9.pdf
Reference7 articles.
1. Al-Hassnan Z. N., Al-Bakheet A., Abu-Dheim N., Al-Younes B., Colak D. and Kaya N. 2011 A novel interstitial microdeletion of 7q22.1-7q22.3 detected by array comparative genomic hybridization. Am. J. Med. Genet. A 155, 3128– 3131.
2. Colella S., Yau C., Taylor J. M., Mirza G., Butler H., Clouston P. et al. 2007 QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Nucl. Acids Res. 35, 2013– 2025.
3. De Preter K., Speleman F., Combaret V., Lunec J., Laureys G., Eussen B. H. J. et al. 2002 Quantification of MYCN, DDX1, and NAG gene copy number in neuroblastoma using a real-time quantitative PCR assay. Mod. Pathol. 15, 159–166.
4. Hoebeeck J., van der Luijt R., Poppe B., De Smet E., Yigit N., Claes K. et al. 2005 Rapid detection of VHL exon deletions using real-time quantitative PCR. Lab. Invest. 85, 24–33.
5. Lybaek H., Meza-Zepeda L. A., Kresse S. H., Høysaeter T., Steen V. M. and Houge G. 2008 Array-CGH fine mapping of minor and cryptic HR-CGH detected genomic imbalances in 80 out of 590 patients with abnormal development. Eur. J. Hum. Genet. 16, 1318–1328.
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