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Original article
A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype

Authors

  1. Correspondence to Dr Christiane Zweier, Institute of Human Genetics, Schwabachanlage 10, Erlangen 91054, Germany; christiane.zweier{at}uk-erlangen.de
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Citation

Zweier C, Kraus C, Brueton L, et al
A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype

Publication history

  • Received July 10, 2013
  • Revised August 15, 2013
  • Accepted August 29, 2013
  • First published October 3, 2013.
Online issue publication 
February 22, 2018

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