DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Cancrini C, Puliafito P, Digilio MC. , et al; Italian Network for Primary Immunodeficiencies.
Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
J Pediatr 2014;
164 (06) 1475-80.e2
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