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Next-generation panel sequencing identifies NF1 germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1.

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author: Graeme Eisenhofer  Aleksander Prejbisz  Laura Gieldon  Barbara Klink  Andreas Rump  Roland Därr  Andrzej Januszewicz  Mercedes Robledo 

Publication date November 20, 2017
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