**The BVMC (U54NS065705) is a part of the National Institutes of Health (NIH) Rare Disease Clinical Research Network (RDCRN), supported through the NIH Office of Rare Diseases Research (ORDR)/National Center for Advancing Translational Sciences (NCATS) and the National Institute of Neurological Disorders and Stroke (NINDS).
Version of Record online: 18 SEP 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Special Issue: SPECIAL ISSUE: GROWTH CHARTS IN GENETIC SYNDROMES
Volume 158A, Issue 11, pages 2829–2834, November 2012
How to Cite
Nishida, T., Faughnan, M. E., Krings, T., Chakinala, M., Gossage, J. R., Young, W. L., Kim, H., Pourmohamad, T., Henderson, K. J., Schrum, S. D., James, M., Quinnine, N., Bharatha, A., terBrugge, K. G. and White, R. I. (2012), Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia: Gene–phenotype correlations. Am. J. Med. Genet., 158A: 2829–2834. doi: 10.1002/ajmg.a.35622
How to Cite this Article: Nishida T, Faughnan ME, Krings T, Chakinala TK, Gossage JR, Young WL, Kim H, Pourmohamad T, Henderson KJ, Schrum SD, James M, Quinnine N, Bharatha A, terBrugge KG, White RIJ, 2012. Brain Arteriovenous malformations associated with hereditary hemorrhagic telangiectasia: Gene-phenotype correlations. Am J Med Genet Part A 158A: 2829–2834.
- Issue online: 17 OCT 2012
- Version of Record online: 18 SEP 2012
- Manuscript Accepted: 26 JUL 2012
- Manuscript Received: 5 JAN 2012
- US Public Health Service, National Institutes of Health (NIH), National Institute of Neurological Disorders and Stroke (NINDS) and Office of Rare Disease Research (ORDR)/National Center for Advancing Translational Sciences (NCATS). Grant Number: U54NS065705
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