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Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocyte leukemia.

Autor: Silva, Maria Luiza Macedo¹ mlmacedosilva@hotmail.com, do Socorro Pombo-de-Oliveira, Maria² mpombo@inca.gov.br, Raimondi, Susana C.³ Susana.Raimondi@stjude.org, Mkrtchyan, Hasmik⁴ hamk@mti.uni-jena.de, Abdelhay, Eliana¹ eabdelhay@inca.gov.br, de Figueiredo, Amanda Faria¹ amandaffbr@yahoo.com.br, de Souza, Mariana Tavares¹ nana•bio•06@hotmail.com, Garcia, Daniela Ribeiro Ney¹ danyneygarcia@yahoo.com.br, de Ventura, Eliane Maria Soares⁵ elianes01@yahoo.com.br, de Sousa, Adriana Martins⁶ emaildaadriana@ig.com.br, Liehr, Thomas⁴ i8lith@mti.uni-jena.de

Publikováno v: Molecular Cytogenetics (17558166). 2009, Vol. 2, p1-6. 6p. 2 Diagrams, 1 Chart.

Intrachromosomal amplification of chromosome 21 (iAMP21) detected by ETV6/RUNX1 FISH screening in childhood acute lymphoblastic leukemia: a case report

Autor: Garcia,Daniela Ribeiro Ney, Arancibia,Alejandro Mauricio, Ribeiro,Raul C., Land,Marcelo Gerardin Poirot, Silva,Maria Luiza Macedo

Publikováno v: Revista Brasileira de Hematologia e Hemoterapia, Volume: 35, Issue: 5, Pages: 369-371, Published: 2013
Revista Brasileira de Hematologia e Hemoterapia v.35 n.5 2013
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC

Chromosome abnormalities that usually define high-risk acute lymphoblastic leukemia are the t(9;22)/ breakpoint cluster region protein-Abelson murine leukemia viral oncogene homolog 1, hypodiploid with < 44 chromosomes and 11q23/ myeloid/lymphoid leu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cc735865b7034fb2d0cba4cae04d3767
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842013000500369&lng=en&tlng=en

Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome

Autor: Hernandes, Marina Araújo Fonzar, Marques-Salles, Terezinha de Jesus, Mkrtchyan, Hasmik, Soares-Ventura, Eliane Maria, Leite, Edinalva Pereira, Muniz, Maria Tereza Cartaxo, Cornélio, Maria Teresa Marquim Nogueira, Liehr, Thomas, Santos, Neide, Silva, Maria Luiza Macedo

Publikováno v: Case Reports in Genetics.

Acute lymphoblastic leukemia (ALL), CD10+ B-cell precursor, represents the most frequent type of childhood ALL from 3 to 6 years of age. The t(12;21)(p13;q22) occurs in 25% of cases of B-cell precursor ALL, it is rare in children less than 24 months

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=hindawi_publ::f4bc4696fb210eb85c95f51396839896

Molecular characterization of KMT2A fusion partner genes in 13 cases of pediatric leukemia with complex or cryptic karyotypes.

Autor: Ney Garcia, Daniela R., Souza, Mariana T., Figueiredo, Amanda F., Othman, Moneeb A. K., Rittscher, Katharina, Abdelhay, Eliana, Capela de Matos, Roberto R., Meyer, Claus, Marschalek, Rolf, Land, Marcelo G. P., Liehr, Thomas, Ribeiro, Raul C., Silva, Maria Luiza Macedo, de Souza, Mariana T, de Figueiredo, Amanda F

Publikováno v: Hematological Oncology; Dec2017, Vol. 35 Issue 4, p760-768, 9p