Ann Lab Med 2018; 38(1): 63-66  
Molecular and Cytogenetic Studies in a Child with Burkitt Lymphoma and Ataxia-Telangiectasia Syndrome Harboring MYC Overexpression and Partial Trisomy 8
Mariana T. De Souza, M.S.1,2, Gabriela Vera-Lozada, Ph.D.2,3, Moneeb Othman, Ph.D.4, Teresinha J. Marques-Salles, Ph.D.5, Luciana W. Pinto, Ph.D.6, Moisés M. da Rocha, B.S.1, Soraia Rouxinol, M.D.7, Thomas Liehr, Ph.D.4, Raul C. Ribeiro, M.D.8,9, Rocio Hassan, Ph.D.2,3, and Maria Luiza M. Silva, Ph.D.1,2
Cytogenetics Department1, Bone Marrow Transplantation Center, Instituto Nacional de Câncer, Rio de Janeiro, RJ, Brazil; Post Graduation Oncology Program2, Instituto Nacional de Câncer, Rio de Janeiro, RJ, Brazil; Oncovirology Laboratory3, Bone Marrow Transplantation Center, Instituto Nacional de Câncer, Rio de Janeiro, RJ, Brazil; Institute of Human Genetics4, Jena University Hospital, Friedrich Schiller University, Jena, TH, Germany; Department of Genetics5, Pernambuco University, Recife, PE, Brazil; Integrated Department of Pathology6, Instituto Nacional de Câncer, Rio de Janeiro, RJ, Brazil; Pediatric Hematology Department7, Hospital Federal da Lagoa, Rio de Janeiro, RJ, Brazil; Department of Oncology8, St. Jude Children’s Research Hospital, Memphis, TN, USA; Instituto Pelé Pequeno Príncipe9, Postgraduate Program in Child Adolescent Health, Curitiba, Paraná, Brazil
Correspondence to: Maria Luiza Macedo Silva
Cytogenetics Department, Instituto Nacional de Câncer (INCA) Praça da Cruz Vermelha, 23 – 6th floor, Rio de Janeiro, RJ, 20.230-130, Brazil
Tel: +55-21-32071701, Fax: +55-21-32076865
E-mail: luizamacedo@inca.gov.br
Received: April 19, 2017; Revised: June 28, 2017; Accepted: September 11, 2017; Published online: January 1, 2018.
© The Korean Society for Laboratory Medicine. All rights reserved.

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