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dc.contributor.authorPoyrazoglu, Şükran
dc.contributor.authorDarendeliler, Feyza
dc.contributor.authorToksoy, Guven
dc.contributor.authorBas, Firdevs
dc.contributor.authorDurmaz, Ozlem
dc.contributor.authorYildiz, Melek
dc.contributor.authorOnal, Zerrin
dc.contributor.authorYesil, Gozde
dc.contributor.authorKabil, Tugce Goksu
dc.date.accessioned2023-05-29T13:29:18Z
dc.date.available2023-05-29T13:29:18Z
dc.identifier.citationYildiz M., Onal Z., Yesil G., Kabil T. G., Toksoy G., Poyrazoglu Ş., Bas F., Durmaz O., Darendeliler F., "A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings.", Journal of clinical research in pediatric endocrinology, 2023
dc.identifier.othervv_1032021
dc.identifier.otherav_33606810-a2fe-4856-b184-f33932f77332
dc.identifier.urihttp://hdl.handle.net/20.500.12627/189037
dc.identifier.urihttps://doi.org/10.4274/jcrpe.galenos.2023.2022-10-4
dc.language.isoeng
dc.titleA Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings.
dc.typeMakale
dc.relation.journalJournal of clinical research in pediatric endocrinology
dc.contributor.department, ,
dc.contributor.firstauthorID4254477


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