Recurrent microdeletions at chromosome 2p11.2 are associated with thymic hypoplasia and features resembling DiGeorge syndrome-Reference-Cited by-同舟云学术

Recurrent microdeletions at chromosome 2p11.2 are associated with thymic hypoplasia and features resembling DiGeorge syndrome

Published:2020-01 Issue:1 Volume:145 Page:358-367.e2
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Bernstock Joshua D.,Totten Arthur H.,Elkahloun Abdel G.,Johnson Kory R.,Hurst Anna C.,Goldman Frederick,Groves Andrew K.,Mikhail Fady M.,Atkinson T. Prescott^ORCID

Funder

UAB

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference31 articles.

1. 22q and two: 22q11.2 deletion syndrome and coexisting conditions;Cohen;Am J Med Genet A,2018

2. Complete DiGeorge syndrome associated with CHD7 mutation;Sanka;J Allergy Clin Immunol,2007

3. Role of TBX1 in human del22q11.2 syndrome;Yagi;Lancet,2003

4. Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder;Liu;Hum Mol Genet,2018

5. Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype;Gottlieb;Am J Hum Genet,1998

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