Clinical Phenotype, Immunological Abnormalities, and Genomic Findings in Patients with DiGeorge Spectrum Phenotype without 22q11.2 Deletion
Author:
Funder
Italian Ministry of Health
Publisher
Elsevier BV
Subject
Immunology and Allergy
Reference32 articles.
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2. 22q11.2 deletion syndrome;McDonald-McGinn;Nat Rev Dis Primers,2015
3. Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome);McDonald-McGinn;Medicine (Baltimore),2011
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