How to cite this article: Francey LJ, Conlin LK, Kadesch HE, Clark D, Berrodin D, Sun Y, Glessner J, Hakonarson H, Jalas C, Landau C, Spinner NB, Kenna M, Sagi M, Rehm HL, Krantz ID. 2012. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Am J Med Genet Part A 158A:298–308.
Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment†
Version of Record online: 6 DEC 2011
Copyright © 2011 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 2, pages 298–308, February 2012
How to Cite
Francey, L. J., Conlin, L. K., Kadesch, H. E., Clark, D., Berrodin, D., Sun, Y., Glessner, J., Hakonarson, H., Jalas, C., Landau, C., Spinner, N. B., Kenna, M., Sagi, M., Rehm, H. L. and Krantz, I. D. (2012), Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. Am. J. Med. Genet., 158A: 298–308. doi: 10.1002/ajmg.a.34391
- Issue online: 19 JAN 2012
- Version of Record online: 6 DEC 2011
- Manuscript Accepted: 14 OCT 2011
- Manuscript Received: 16 FEB 2011
- NIDCD (IDK). Grant Numbers: R33DC008630, R33DC008630-03S1
- CHOP Institutional Development Funds (IDK)
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