Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome
Author:
Affiliation:
1. The Division of Clinical Genetics; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania
2. The Division of Allergy Immunology; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38597/fullpdf
Reference56 articles.
1. Clinical features of 78 adults with 22q11 deletion syndrome;Bassett;American Journal of Medical Genetics Part A,2005
2. Rare genome-Wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome;Bassett;American Journal of Psychiatry,2017
3. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;The Journal of Pediatrics,2011
4. Antibody deficiency in adults with 22q11.2 deletion syndrome;Bjork;American Journal of Medical Genetics Part A,2012
5. A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population;Botto;Pediatrics,2003
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