Segmental Duplications and Copy-Number Variation in the Human Genome
The American Journal of Human Genetics2005Vol. 77(1), pp. 78–88
Citations Over TimeTop 1% of 2005 papers
Andrew J. Sharp, Devin P. Locke, Sean McGrath, Ze Cheng, Jeffrey A. Bailey, Rhea U. Vallente, L.M. Pertz, Royden A. Clark, Stuart Schwartz, Rick Segraves, Vanessa V. Oseroff, Donna G. Albertson, Daniel Pinkel, Evan E. Eichler
Related Papers
- → Detection of clinically relevant exonic copy-number changes by array CGH(2010)237 cited
- → Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome(2006)72 cited
- → MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization(2012)9 cited
- → [Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].(2012)7 cited
- → [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].(2011)