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

AIM: 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,...

詳細記述

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書誌詳細
出版年:Turk Pediatri Ars
主要な著者: Nepesov, Serdar, Aygün, Fatma Deniz, Küçüksezer, Umut, Taşdemir, Emre, Çokuğraş, Haluk, Camcıoğlu, Yıldız
フォーマット: Artigo
言語:Inglês
出版事項: Kare Publishing 2019
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6559977/
https://ncbi.nlm.nih.gov/pubmed/31217706
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/TurkPediatriArs.2019.95815
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