Iranian Journal of Pediatrics

Published by: Kowsar

Williams-Beuren Syndrome: A Case Confirmed by Array-CGH Method

MinYan Jiang 1 , * and Li Liu 1
Authors Information
1 Department of Endocrinology and Metabolisms, Guangzhou Women and Children’s Medical Center, Guangzhou, China
Article information
  • Iranian Journal of Pediatrics: February 28, 2015, 25 (1)
  • Published Online: February 21, 2015
  • Article Type: Letter
  • Received: October 1, 2014
  • Accepted: November 14, 2014
  • DOI: 10.5812/ijp.247

To Cite: Jiang M, Liu L. Williams-Beuren Syndrome: A Case Confirmed by Array-CGH Method, Iran J Pediatr. 2015 ;25(1):-. doi: 10.5812/ijp.247.

Copyright © 2015, Growth & Development Research Center.This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
References
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  • 2. Beuren AJ, Apitz J, Harmjanz D. Supravalvular aortic stenosis in association with mental retardation and a certain facial appearance. Circulation. 1962; 26: 1235-40[PubMed]
  • 3. Schubert C. The genomic basis of the Williams-Beuren syndrome. Cell Mol Life Sci. 2009; 66(7): 1178-97[DOI][PubMed]
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  • 6. Peoples R, Perez-Jurado L, Wang YK, Kaplan P, Francke U. The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion. Am J Hum Genet. 1996; 58(6): 1370-3[PubMed]
  • 7. Ferrero GB, Biamino E, Sorasio L, Banaudi E, Peruzzi L, Forzano S, di Cantogno LV, Silengo MC, et al. Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients. Eur J Med Genet. 2007; 50(5): 327-37[DOI][PubMed]
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