Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution’s experience
Serdar Nepesov, Fatma Deniz Aygün, Umut Küçüksezer, Emre Taşdemir, Haluk Çokuğraş, Yıldız Camcıoğlu
(Turk Arch Pediatr 2019; 54: 28-34) DOI: 10.14744/TurkPediatriArs.2019.95815