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Mutations in <i>AR</i> or <i>SRD5A2</i> Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children With 46,XY DSD.

dc.contributor.authorAkcan, Nese
dc.contributor.authorDarendeliler, Feyza
dc.contributor.authorAvci, Sahin
dc.contributor.authorAbali, Zehra Yavas
dc.contributor.authorPoyrazoglu, Sukran
dc.contributor.authorAghayev, Agharza
dc.contributor.authorKaraman, Volkan
dc.contributor.authorBundak, Ruveyde
dc.contributor.authorBasaran, Seher
dc.contributor.authorBas, Firdevs
dc.contributor.authorUyguner, Z. Oya
dc.contributor.authorAltunoglu, Umut
dc.contributor.authorToksoy, Güven
dc.contributor.authorKaraman, Birsen
dc.date.accessioned2022-02-18T09:44:56Z
dc.date.available2022-02-18T09:44:56Z
dc.identifier.citationAkcan N., Uyguner Z. O. , Bas F., Altunoglu U., Toksoy G., Karaman B., Avci S., Abali Z. Y. , Poyrazoglu S., Aghayev A., et al., "Mutations in <i>AR</i> or <i>SRD5A2</i> Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children With 46,XY DSD.", Journal of clinical research in pediatric endocrinology, 2022
dc.identifier.issn1308-5727
dc.identifier.otherav_5acaea80-24fe-4014-b081-0403ba67f688
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177902
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/5acaea80-24fe-4014-b081-0403ba67f688/file
dc.identifier.urihttps://doi.org/10.4274/jcrpe.galenos.2021.2021-9-19
dc.language.isoeng
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectGeneral Medicine
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectTıbbi Genetik
dc.subjectGenetics
dc.subjectFamily Practice
dc.subjectGenetics (clinical)
dc.subjectFundamentals and Skills
dc.subjectKlinik Tıp (MED)
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTIP, GENEL & İÇECEK
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleMutations in <i>AR</i> or <i>SRD5A2</i> Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children With 46,XY DSD.
dc.typeMakale
dc.relation.journalJournal of clinical research in pediatric endocrinology
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.contributor.firstauthorID3390675


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