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Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.

dc.contributor.authorTasdemir, Emre
dc.contributor.authorKucuksezer, Umut Can
dc.contributor.authorCamcioglu, Yildiz
dc.contributor.authorAygun, Fatma Deniz
dc.contributor.authorNepesov, Serdar
dc.contributor.authorCokugras, Haluk
dc.date.accessioned2021-03-05T20:58:04Z
dc.date.available2021-03-05T20:58:04Z
dc.date.issued2019
dc.identifier.citationNepesov S., Aygun F. D. , Kucuksezer U. C. , Tasdemir E., Cokugras H., Camcioglu Y., "Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.", Turk pediatri arsivi, cilt.54, ss.28-34, 2019
dc.identifier.othervv_1032021
dc.identifier.otherav_d6ada86e-3dbf-486d-8548-65117a8170cf
dc.identifier.urihttp://hdl.handle.net/20.500.12627/141666
dc.identifier.urihttps://doi.org/10.14744/turkpediatriars.2019.95815
dc.description.abstractAim: The aim of this study was to identify the clinical and immunologic features of patients with 22q11.2 deletion syndrome who were followed up in our clinic Thus, it is aimed to identify the syndrome early, choose the right treatment options according to humoral and cellular immunologic analysis, and enlighten how to follow up these kinds of patients with immunodeficiencies.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.titleClinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.
dc.typeMakale
dc.relation.journalTurk pediatri arsivi
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume54
dc.identifier.issue1
dc.identifier.startpage28
dc.identifier.endpage34
dc.contributor.firstauthorID262806


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