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Special feature on copy-number variation
Original article
Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype

Authors

  1. Correspondence to Dr Meena Balasubramanian, Sheffield Clinical Genetics Service, Sheffield NHS Foundation Trust, Western Bank, Sheffield S10 2TH, UK; meena.balasubramanian{at}nhs.net
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Citation

Balasubramanian M, Smith K, Basel-Vanagaite L, et al
Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype
Journal of Medical Genetics 2011;48:290-298.

Publication history

  • Received August 28, 2010
  • Revised October 7, 2010
  • Accepted October 8, 2010
  • First published February 22, 2011.
Online issue publication 
April 27, 2011

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