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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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Bibliografische gegevens
Gepubliceerd in:Turk Pediatri Ars
Hoofdauteurs: Nepesov, Serdar, Aygün, Fatma Deniz, Küçüksezer, Umut, Taşdemir, Emre, Çokuğraş, Haluk, Camcıoğlu, Yıldız
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Kare Publishing 2019
Onderwerpen:
Online toegang: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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