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Paper Details

Recurrent microdeletions at chromosome 2p11.2 are associated with thymic hypoplasia and features resembling DiGeorge syndrome.
J Allergy Clin Immunol
21
2020
DiGeorge syndrome, FOXI3, FOXN1, Patients, T, T- and B-cell subsets, T-cell lymphopenia, T-cell receptor, Thymic hypoplasia/aplasia, candidate gene, chromosomal microarray, chromosome 2p11, combined immunodeficiency, epithelial adherens junctions, epithelial cells, forkhead, forkhead box I3, forkhead box N1, haploinsufficiency for FOXI3, human, immunoglobulin kappa light chain locus, mice, mouse, mouse knockout strain, patients, selective T-cell lymphopenia, splenocytes, thymic RNA, thymic hypoplasia, thymocytes, wild
Author NameAffiliation
Abdel G ElkahlounNational Human Genome Research Institute, National Institutes of Health
Anna C E HurstUniversity of Alabama at Birmingham
Andrew K GrovesBaylor College of Medicine
Fady M MikhailUniversity of Alabama at Birmingham
Fady M MikhailUniversity of Alabama at Birmingham
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