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Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods

dc.contributor.authorYÜKSEL APAK, MEMNUNE
dc.contributor.authorWOLLNIK, B
dc.contributor.authorTükel, Turgut
dc.contributor.authorUYGUNER, O
dc.contributor.authorKAYSERILI, HÜLYA
dc.contributor.authorATALAR, Fatmahan
dc.date.accessioned2021-03-05T08:52:11Z
dc.date.available2021-03-05T08:52:11Z
dc.identifier.citationATALAR F., Tükel T., YÜKSEL APAK M., UYGUNER O., KAYSERILI H., WOLLNIK B., "Investigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods", VI. Ulusal Tibbi Genetik Kongresi, Antalya, Türkiye, ss.53
dc.identifier.othervv_1032021
dc.identifier.otherav_9b18d7a8-a561-43e4-ba3f-bc128d69ba4e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/104257
dc.language.isotur
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.titleInvestigation of CYP21 gene mutations in congenital adrenal hyperplasia due to steroid 21 Hydroxilase Deficiency-old vs new diagnostic methods
dc.typeBildiri
dc.contributor.departmentİstanbul Üniversitesi , Çocuk Sağlığı Enstitüsü , Dahili Tıp Bilimleri Bölümü
dc.contributor.firstauthorID630023


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