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Journal of Clinical Immunology
Literature
1.
Edelmann L, Pandita RK, Spiteri E, et al. A common molecular basis for rearrangement disorders on chromosome 22q11. Hum Mol Genet. 1999;8(7):1157–67.CrossRefPubMed
2.
Portnoi MF. Microduplication 22q11.2: a new chromosomal syndrome. Eur J Med Genet. 2009;52(2-3):88–93.CrossRefPubMed
3.
Ensenauer RE, Adeyinka A, Flynn HC, et al. Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients. Am J Hum Genet. 2003;73(5):1027–40.CrossRefPubMedPubMedCentral
4.
Engels H, Brockschmidt A, Hoischen A, et al. DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation. Neurology. 2007;68(10):743–50.CrossRefPubMed
Metadata
Title
Immunodeficiency in a Child with 22q11.2 Microduplication Syndrome
Authors
Robyn Traynor
Karina M. Butler
Andrew J. Cant
Timothy Ronan Leahy
Publication date
01-07-2016
Publisher
Springer US
Published in
Journal of Clinical Immunology / Issue 5/2016
Print ISSN: 0271-9142
Electronic ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-016-0286-1

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Erratum to: Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

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Into Action: Improving Access to Optimum Care for all Primary Immunodeficiency Patients

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Respiratory Health and Related Quality of Life in Patients with Congenital Agammaglobulinemia in the Northern Region of the UK

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A Case of SLC29A3 Spectrum Disorder—Unresponsive to Multiple Immunomodulatory Therapies

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