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Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations.
J Allergy Clin Immunol. 2022 Oct;150(4):947-954. doi: 10.1016/j.jaci.2022.06.009. Epub 2022 Jun 24.
J Allergy Clin Immunol. 2022.
PMID: 35753512
Free PMC article.
Review.
The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome.
Jevtich K, Price S, Similuk M, Kulm E, Yan J, Setzer M, Jamal L, Franco LM, Ghosh R, Walkiewicz M, Rao VK.
Jevtich K, et al.
Blood Adv. 2022 Jul 12;6(13):3974-3978. doi: 10.1182/bloodadvances.2021005835.
Blood Adv. 2022.
PMID: 35476126
Free PMC article.
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Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity.
Beers BJ, Similuk MN, Ghosh R, Seifert BA, Jamal L, Kamen M, Setzer MR, Jodarski C, Duncan R, Hunt D, Mixer M, Cao W, Bi W, Veltri D, Karlins E, Zhang L, Li Z, Oler AJ, Jevtich K, Yu Y, Hullfish H, Bielekova B, Frischmeyer-Guerrerio P, Dang Do A, Huryn LA, Olivier KN, Su HC, Lyons JJ, Zerbe CS, Rao VK, Keller MD, Freeman AF, Holland SM, Franco LM, Walkiewicz MA, Yan J.
Beers BJ, et al. Among authors: jevtich k.
Front Immunol. 2023 May 5;14:1172004. doi: 10.3389/fimmu.2023.1172004. eCollection 2023.
Front Immunol. 2023.
PMID: 37215141
Free PMC article.
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