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Branchio–oto–renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses
Kirsten Marie Sanggaard, Nanna Dahl Rendtorff, Klaus Wilbrandt Kjaer, Hans Eiberg, Torsten Johnsen, Steen Gimsing, Jørgen Dyrmose, Kristian Otto Nielsen, Kasper Lage and Lisbeth Tranebjærg
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