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  • Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification

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Original article
Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification

Authors

  1. Correspondence to:
 C L Harteveld
 Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands; C.L.Harteveld{at}LUMC.nl
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Citation

Harteveld CL, Voskamp A, Phylipsen M, et al
Nine unknown rearrangements in 16p13.3 and 11p15.4 causing α- and β-thalassaemia characterised by high resolution multiplex ligation-dependent probe amplification
Journal of Medical Genetics 2005;42:922-931.

Publication history

  • Accepted May 4, 2005
  • Revised May 3, 2005
  • First published May 13, 2005.
Online issue publication 
April 27, 2016

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Copyright 2005 Journal of Medical Genetics