TY  - JOUR
AU  - Gieldon, Laura
AU  - William, Doreen
AU  - Hackmann, Karl
AU  - Jahn, Winnie
AU  - Jahn, Arne
AU  - Wagner, Johannes
AU  - Rump, Andreas
AU  - Bechmann, Nicole
AU  - Nölting, Svenja
AU  - Knösel, Thomas
AU  - Gudziol, Volker
AU  - Constantinescu, Georgiana
AU  - Masjkur, Jimmy
AU  - Beuschlein, Felix
AU  - Timmers, Henri Jlm
AU  - Canu, Letizia
AU  - Pacak, Karel
AU  - Robledo Mercedes, Mercedes
AU  - Aust, Daniela
AU  - Schröck, Evelin
AU  - Eisenhofer, Graeme
AU  - Richter, Susan
AU  - Klink, Barbara
PY  - 2019
DO  - 10.3390/cancers11060809
SN  - 2072-6694
UR  - http://hdl.handle.net/20.500.12105/7833
AB  - Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors with a strong hereditary background and a large genetic heterogeneity. Identification of the underlying genetic cause is crucial for the management of patients and their...
LA  - eng
PB  - Multidisciplinary Digital Publishing Institute (MDPI)
KW  - CNV detection
KW  - Hereditary
KW  - Next-generation sequencing
KW  - Paraganglioma
KW  - Pheochromocytoma
KW  - Sporadic
TI  - Optimizing Genetic Workup in Pheochromocytoma and Paraganglioma by Integrating Diagnostic and Research Approaches
TY  - journal article
ER  -