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No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia
  1. Correspondence to:
 Dr Marwan Shinawi
 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; mshinawibcm.tmc.edu
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Citation

Karabegovic A, Shinawi M, Cymerman U, et al
No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia

Publication history

  • Received July 7, 2004
  • Accepted July 8, 2004
  • First published November 1, 2004.
Online issue publication 
April 27, 2016

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