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2018 | 2 |
2020 | 1 |
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Page 1
Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2.
Mol Syndromol. 2018 May;9(3):164-169. doi: 10.1159/000488820. Epub 2018 Apr 28.
Mol Syndromol. 2018.
PMID: 29928183
Free PMC article.
Identification of clinically relevant phenotypes in patients with Ebstein anomaly.
Cabrera R, Miranda-Fernández MC, Huertas-Quiñones VM, Carreño M, Pineda I, Restrepo CM, Silva CT, Quero R, Cano JD, Manrique DC, Camacho C, Tabares S, García A, Sandoval N, Moreno Medina KJ, Dennis Verano RJ.
Cabrera R, et al. Among authors: quero r.
Clin Cardiol. 2018 Mar;41(3):343-348. doi: 10.1002/clc.22870. Epub 2018 Mar 22.
Clin Cardiol. 2018.
PMID: 29569399
Free PMC article.
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Immunodeficiency in a Patient with 22q11.2 Distal Deletion Syndrome and a p.Ala7dup Variant in the MAPK1 Gene.
Sánchez AI, García-Acero MA, Paredes A, Quero R, Ortega RI, Rojas JA, Herrera D, Parra M, Prieto K, Ángel J, Rodríguez LS, Prieto JC, Franco M.
Sánchez AI, et al. Among authors: quero r.
Mol Syndromol. 2020 Feb;11(1):15-23. doi: 10.1159/000506032. Epub 2020 Feb 5.
Mol Syndromol. 2020.
PMID: 32256297
Free PMC article.
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