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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D. Aust | A. Rump | B. Klink | A. Tzschach | K. Hackmann | A. Januszewicz | G. Eisenhofer | M. Robledo | Silke Zeugner | S. Richter | E. Schrock | A. Prejbisz | J. Masjkur | L. Gieldon | M. Lahera | R. Därr