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Partial 1q Duplications and Associated Phenotype.
Morris ML, Baroneza JE, Teixeira P, Medina CT, Cordoba MS, Versiani BR, Roese LL, Freitas EL, Fonseca AC, Dos Santos MC, Pic-Taylor A, Rosenberg C, Oliveira SF, Ferrari I, Mazzeu JF. Morris ML, et al. Among authors: versiani br. Mol Syndromol. 2016 Feb;6(6):297-303. doi: 10.1159/000443599. Epub 2016 Feb 4. Mol Syndromol. 2016. PMID: 27022331 Free PMC 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: versiani br. Mol Syndromol. 2022 Jul;13(4):290-304. doi: 10.1159/000518872. Epub 2022 Feb 11. Mol Syndromol. 2022. PMID: 36158055 Free PMC article.
Syndromic hearing loss molecular diagnosis: Application of massive parallel sequencing.
Soares de Lima Y, Chiabai M, Shen J, Córdoba MS, Versiani BR, Benício ROA, Pogue R, Mingroni-Netto RC, Lezirovitz K, Pic-Taylor A, Mazzeu JF, Oliveira SF. Soares de Lima Y, et al. Among authors: versiani br. Hear Res. 2018 Dec;370:181-188. doi: 10.1016/j.heares.2018.10.008. Epub 2018 Oct 16. Hear Res. 2018. PMID: 30390570
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome.
Montenegro LR, Silveira LF, Tusset C, de Castro M, Versiani BR, Latronico AC, Mendonca BB, Trarbach EB. Montenegro LR, et al. Among authors: versiani br. Fertil Steril. 2013 Sep;100(3):854-9. doi: 10.1016/j.fertnstert.2013.04.045. Epub 2013 May 28. Fertil Steril. 2013. PMID: 23721716 Free article.
15 results