How to Cite this Article: Nathanson J, Swarr DT, Singer A, Liu M, Chinn A, Jones W, Hurst J, Khalek N, Zackai E, Slavotinek A. 2013. Novel FREM1 mutations expand the phenotypic spectrum associated with manitoba-oculo-tricho-anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (BNAR) syndrome. Am J Med Genet Part A 161A: 473–478.
Novel FREM1 mutations expand the phenotypic spectrum associated with manitoba-oculo-tricho-anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (BNAR) syndrome†
Article first published online: 8 FEB 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 3, pages 473–478, March 2013
How to Cite
Nathanson, J., Swarr, D. T., Singer, A., Liu, M., Chinn, A., Jones, W., Hurst, J., Khalek, N., Zackai, E. and Slavotinek, A. (2013), Novel FREM1 mutations expand the phenotypic spectrum associated with manitoba-oculo-tricho-anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (BNAR) syndrome. Am. J. Med. Genet., 161: 473–478. doi: 10.1002/ajmg.a.35736
- Issue published online: 21 FEB 2013
- Article first published online: 8 FEB 2013
- Manuscript Accepted: 16 SEP 2012
- Manuscript Received: 26 JUL 2012
- Eunice Kennedy Shriver National Institute of Child Health. Grant Number: K08HD053476-01A1
- National Institutes of Health
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