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A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).
de Figueiredo AF, Vieira TP, Liehr T, Bhatt S, de Souza MT, Binato R, Marques-Salles Tde J, Carboni E, Ribeiro RC, Silva ML, Abdelhay E. de Figueiredo AF, et al. Among authors: vieira tp. Leuk Res. 2012 Apr;36(4):e74-7. doi: 10.1016/j.leukres.2011.12.009. Epub 2012 Jan 18. Leuk Res. 2012. PMID: 22261229 No abstract available.
A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.
Ney-Garcia DR, Vieira TP, Liehr T, Bhatt S, de Souza MT, de Figueiredo AF, Ribeiro RC, Silva ML. Ney-Garcia DR, et al. Among authors: vieira tp. Blood Cells Mol Dis. 2013 Feb;50(2):131-3. doi: 10.1016/j.bcmd.2012.09.005. Epub 2012 Oct 6. Blood Cells Mol Dis. 2013. PMID: 23044159 No abstract available.
Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion.
Guilherme RS, Soares KC, Simioni M, Vieira TP, Gil-da-Silva-Lopes VL, Kim CA, Brunoni D, Spinner NB, Conlin LK, Christofolini DM, Kulikowski LD, Steiner CE, Melaragno MI. Guilherme RS, et al. Among authors: vieira tp. Am J Med Genet A. 2014 Jul;164A(7):1659-65. doi: 10.1002/ajmg.a.36512. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700634 Review.
Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia.
Simioni M, Vieira TP, Sgardioli IC, Freitas EL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Gil-da-Silva-Lopes VL. Simioni M, et al. Among authors: vieira tp. Am J Med Genet A. 2012 Nov;158A(11):2905-10. doi: 10.1002/ajmg.a.35603. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991255
Atypical copy number abnormalities in 22q11.2 region: report of three cases.
Molck MC, Vieira TP, Sgardioli IC, Simioni M, Dos Santos AP, Souza J, Monteiro FP, Gil-da-Silva-Lopes VL. Molck MC, et al. Among authors: vieira tp. Eur J Med Genet. 2013 Sep;56(9):515-20. doi: 10.1016/j.ejmg.2013.07.002. Epub 2013 Jul 23. Eur J Med Genet. 2013. PMID: 23886712 Free article.
A boy with partial dup(18q)/del(18p) due to a maternal pericentric inversion: Genotype-phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature.
Lustosa-Mendes E, Dos Santos AP, Viguetti-Campos NL, Vieira TP, Gil-da-Silva-Lopes VL. Lustosa-Mendes E, et al. Among authors: vieira tp. Am J Med Genet A. 2017 Jan;173(1):143-150. doi: 10.1002/ajmg.a.37976. Epub 2016 Sep 15. Am J Med Genet A. 2017. PMID: 27633903 Review.
45 results