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A case report of Pituitary Stalk Interruption Syndrome caused by novel compound heterozygous mutations in the KATNIP gene

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dc.contributor.authorBahar S.
dc.contributor.authorÖzgen İ. T.
dc.contributor.authorUyanık B.
dc.contributor.institutionauthorBAHAR, Semra
dc.contributor.institutionauthorÖZGEN, İLKER TOLGA
dc.contributor.institutionauthorUYANIK, BÜLENT
dc.date.accessioned2023-01-08T22:12:45Z
dc.date.available2023-01-08T22:12:45Z
dc.date.issued2022-09-15
dc.identifier.citationBahar S., Özgen İ. T., Uyanık B., \"A case report of Pituitary Stalk Interruption Syndrome caused by novel compound heterozygous mutations in the KATNIP gene\", 60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Rome, İtalya, 15 - 17 Eylül 2022, cilt.95, ss.333-334
dc.identifier.doi10.1159/000525606
dc.identifier.urihttps://avesis.bezmialem.edu.tr/api/publication/314d67c9-cf51-46f3-a8b3-dd64efde620e/file
dc.identifier.urihttps://hdl.handle.net/20.500.12645/34693
dc.relation.ispartof60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectMedicine
dc.subjectHealth Sciences
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectClinical Medicine (MED)
dc.subjectCLINICAL MEDICINE
dc.titleA case report of Pituitary Stalk Interruption Syndrome caused by novel compound heterozygous mutations in the KATNIP gene
dc.typeconferenceObject
dspace.entity.typePublication
local.avesis.id314d67c9-cf51-46f3-a8b3-dd64efde620e
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