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HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype
dc.contributor.authorFang, Qing
dc.contributor.authorBenedetti, Anna Flavia Figueredo
dc.contributor.authorMa, Qianyi
dc.contributor.authorGregory, Louise
dc.contributor.authorLi, Jun Z.
dc.contributor.authorDattani, Mehul
dc.contributor.authorSadeghi‐nejad, Abdollah
dc.contributor.authorArnhold, Ivo J.P.
dc.contributor.authorMendonca, Berenice Bilharinho
dc.contributor.authorCamper, Sally A.
dc.contributor.authorCarvalho, Luciani R.
dc.date.accessioned2016-10-17T21:19:56Z
dc.date.available2017-11-01T15:31:29Zen
dc.date.issued2016-09
dc.identifier.citationFang, Qing; Benedetti, Anna Flavia Figueredo; Ma, Qianyi; Gregory, Louise; Li, Jun Z.; Dattani, Mehul; Sadeghi‐nejad, Abdollah ; Arnhold, Ivo J.P.; Mendonca, Berenice Bilharinho; Camper, Sally A.; Carvalho, Luciani R. (2016). "HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype." Clinical Endocrinology 85(3): 408-414.
dc.identifier.issn0300-0664
dc.identifier.issn1365-2265
dc.identifier.urihttps://hdl.handle.net/2027.42/134248
dc.publisherWiley Periodicals, Inc.
dc.titleHESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype
dc.typeArticleen_US
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelInternal Medicine and Specialties
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/134248/1/cen13067.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/134248/2/cen13067_am.pdf
dc.identifier.doi10.1111/cen.13067
dc.identifier.sourceClinical Endocrinology
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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