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Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management

dc.contributor.authorHermsen, Mario 
dc.contributor.authorSevilla García, María Agustina 
dc.contributor.authorLlorente Pendás, José Luis 
dc.contributor.authorWeiss, Marjan M.
dc.contributor.authorGrimbergen, Anneliese E. M.
dc.contributor.authorAllonca Campa, Eva 
dc.contributor.authorGarcía Inclán, Cristina 
dc.contributor.authorBalbín Felechosa, Milagros 
dc.contributor.authorSuárez Nieto, Carlos 
dc.date.accessioned2016-03-22T13:15:51Z
dc.date.available2016-03-22T13:15:51Z
dc.date.issued2010
dc.identifier.citationCellular Oncology, 32(4), p. 275-283 (2010); doi:10.3233/CLO-2009-0498
dc.identifier.issn1570-5870
dc.identifier.urihttp://hdl.handle.net/10651/36175
dc.format.extentp. 275-283
dc.language.isoeng
dc.relation.ispartofCellular Oncology
dc.rights© 2010 - IOS Press and the authors.
dc.sourceScopus
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-77953449767&partnerID=40&md5=70b360d256e70bd999bbf39c43512243
dc.titleRelevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management
dc.typejournal article
dc.identifier.doi10.3233/CLO-2009-0498
dc.relation.publisherversionhttp://dx.doi.org/10.3233/CLO-2009-0498


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