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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,...

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Detalhes bibliográficos
Publicado no:Turk Pediatri Ars
Main Authors: Nepesov, Serdar, Aygün, Fatma Deniz, Küçüksezer, Umut, Taşdemir, Emre, Çokuğraş, Haluk, Camcıoğlu, Yıldız
Formato: Artigo
Idioma:Inglês
Publicado em: Kare Publishing 2019
Assuntos:
Acesso em linha: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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