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A novel founder BBS1 mutation explains a unique high prevalence of Bardet–Biedl syndrome in the Faroe Islands
  1. Dr T D Hjortshøj, Kennedy Center, Gl. Landevej 7, DK-2600 Glostrup, Denmark; tid{at}kennedy.dk
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Hjortshøj TD, Grønskov K, Brøndum-Nielsen K, et al
A novel founder BBS1 mutation explains a unique high prevalence of Bardet–Biedl syndrome in the Faroe Islands

Publication history

  • Accepted May 31, 2008
  • First published July 31, 2008.
Online issue publication 
February 24, 2009

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