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Primary hyperparathyroidism: disease of diverse genetic, symptomatic, and biochemical phenotypes

dc.contributor.authorMedina, J. E.
dc.contributor.authorRandolph, G. W.
dc.contributor.authorAngelos, P.
dc.contributor.authorZafereo, M. E.
dc.contributor.authorTufano, R. P.
dc.contributor.authorKowalski, L. P.
dc.contributor.authorMontenegro, F. L. M.
dc.contributor.authorOwen, R. P.
dc.contributor.authorKhafif, A.
dc.contributor.authorSuárez Nieto, Carlos 
dc.contributor.authorShaha, A. R.
dc.contributor.authorRodrigo Tapia, Juan Pablo 
dc.contributor.authorKrempl, G. A.
dc.contributor.authorRinaldo, A.
dc.contributor.authorSilver, C. E.
dc.contributor.authorFerlito, A.
dc.date.accessioned2022-03-11T07:29:25Z
dc.date.available2022-03-11T07:29:25Z
dc.date.issued2021
dc.identifier.citationHead and neck, 43(12), p. 3996-4009 (2021); doi:10.1002/hed.26861
dc.identifier.issn1043-3074
dc.identifier.urihttp://hdl.handle.net/10651/62167
dc.format.extentp. 3996-4009
dc.language.isoeng
dc.relation.ispartofHead and neck
dc.rights© Medina, J. E.et al.
dc.sourceScopus
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85115099232&doi=10.1002%2fhed.26861&partnerID=40&md5=2f5479ef3e896582cb01922f185cc087
dc.titlePrimary hyperparathyroidism: disease of diverse genetic, symptomatic, and biochemical phenotypes
dc.typejournal article
dc.identifier.doi10.1002/hed.26861
dc.relation.publisherversionhttp://dx.doi.org/10.1002/hed.26861


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