Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference80 articles.
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3. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis;Driscoll;J. Med. Genet.,1993
4. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations;Ravnan;Am. J. Med. Genet.,1996
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1. Prognostic changes in lymphocyte subpopulations during the development of autoimmune complications in patients with DiGeorge syndrome;Medical Immunology (Russia);2024-07-26
2. Variants in Candidate Genes for Phenotype Heterogeneity in Patients with the 22q11.2 Deletion Syndrome;Genetics Research;2024-03-30
3. Inflammatory Proteomic Analysis of 22q11.2 Deletion Syndrome;Journal of Clinical Immunology;2024-03-15
4. Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome;Metabolomics;2024-02-28
5. Th1/interferon-γ bias in 22q11.2 deletion syndrome is driven by memory T cells and exacerbated by IL-7;Clinical Immunology;2023-11
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