Systematic genetic screening in a prospective group of Danish patients with pheochromocytoma

Recent guidelines recommend consideration of genetic screening in all newly diagnosed patients with pheochromocytoma. Patients diagnosed with pheochromocytoma in the Region of Southern Denmark during 2006–2013 without previously recognized monogenetic etiology were offered genetic screening for muta...

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Detalles Bibliográficos
Autores principales: Hansen, Morten Steen Svarer, Jacobsen, Niels, Frederiksen, Anja Lisbeth, Lund, Lars, Andersen, Marianne Skovsager, Glintborg, Dorte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499796/
https://www.ncbi.nlm.nih.gov/pubmed/28721348
http://dx.doi.org/10.2147/RRU.S134385

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499796/
https://www.ncbi.nlm.nih.gov/pubmed/28721348
http://dx.doi.org/10.2147/RRU.S134385

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