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22q11.2 Deletion and Duplication Syndromes and COVID-19.
Crowley TB, McGinn DM, Sullivan KE; International q11.2 COVID group report. Crowley TB, et al. J Clin Immunol. 2022 May;42(4):746-748. doi: 10.1007/s10875-022-01246-0. Epub 2022 Mar 18. J Clin Immunol. 2022. PMID: 35301601 Free PMC article. No abstract available.
Chromatin Modifications in 22q11.2 Deletion Syndrome.
Zhang Z, Shi L, Song L, Maurer K, Zhao X, Zackai EH, McGinn DE, Crowley TB, McGinn DMM, Sullivan KE. Zhang Z, et al. J Clin Immunol. 2021 Nov;41(8):1853-1864. doi: 10.1007/s10875-021-01123-2. Epub 2021 Aug 25. J Clin Immunol. 2021. PMID: 34435264
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.
Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon T, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Zackai E, Wang T, Shprintzen R, Emanuel BS, Morrow BE; International Chromosome 22q11.2 Consortium. Herman SB, et al. Am J Med Genet A. 2012 Nov;158A(11):2781-7. doi: 10.1002/ajmg.a.35512. Epub 2012 Oct 3. Am J Med Genet A. 2012. PMID: 23034814 Free PMC article.