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Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter.
Faria RS, de Oliveira CP, da Costa MM, da S Rosa MT, Córdoba MS, Pic-Taylor A, Ferrari I, de Oliveira SF, Mazzeu JF. Faria RS, et al. Among authors: de oliveira sf, de oliveira cp. Cytogenet Genome Res. 2016;148(2-3):174-8. doi: 10.1159/000445853. Epub 2016 Jun 2. Cytogenet Genome Res. 2016. PMID: 27251740
Expanding the spectrum of TBL1XR1 deletion: Report of a patient with brain and cardiac malformations.
Vaqueiro AC, de Oliveira CP, Cordoba MS, Versiani BR, de Carvalho CX, Alves Rodrigues PG, de Oliveira SF, Mazzeu JF, Pic-Taylor A. Vaqueiro AC, et al. Among authors: de carvalho cx, de oliveira sf, de oliveira cp. Eur J Med Genet. 2018 Jan;61(1):29-33. doi: 10.1016/j.ejmg.2017.10.008. Epub 2017 Oct 14. Eur J Med Genet. 2018. PMID: 29038029 Free article.
Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review.
de Souza VS, da Cunha GCR, Versiani BR, de Oliveira CP, Rosa MTAS, de Oliveira SF, Moretti PN, Mazzeu JF, Pic-Taylor A. de Souza VS, et al. Among authors: de oliveira sf, de oliveira cp. Mol Syndromol. 2022 Jul;13(4):290-304. doi: 10.1159/000518872. Epub 2022 Feb 11. Mol Syndromol. 2022. PMID: 36158055 Free PMC article.
89 results