Conflict of interest: none.
PECONPI: A novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders
Article first published online: 29 JUL 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 9, pages 2134–2147, September 2013
How to Cite
2013. PECONPI: A novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. Am J Med Genet Part A 161A:2134–2147., , , , , , , , , , , , , , , , .
Ellen A. Tsai, Micah A. Berman, Laura K. Conlin contributed equally to this work.
- Issue published online: 14 AUG 2013
- Article first published online: 29 JUL 2013
- Manuscript Accepted: 11 APR 2013
- Manuscript Received: 2 NOV 2012
- NIH/NIDCD. Grant Numbers: R01DC005247, R33DC008630, U01HG006546
- Ring Chromosome 20 Foundation Grant. Grant Numbers: T32HG000046, T32DC005363, T32GM008638
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