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An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
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An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia

Lovatel, Viviane Lamim ; de Souza, Daiane Corrêa ; Alvarenga, Tatiana Fonseca ; Capela de Matos, Roberto R ; Diniz, Claudia ; Schramm, Marcia Trindade ; Llerena Júnior, Juan Clinton ; Silva, Maria Luiza Macedo ; Abdelhay, Eliana ; de Souza Fernandez, Teresa

Molecular cytogenetics, 2018, Vol.11, p.40-40

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2
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome
Material Type:
Report
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A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome

de Souza, Daiane Correa ; de Figueiredo, Amanda Faria ; Ney Garcia, Daniela R ; da Costa, Elaine Sobral ; Othman, Moneeb A K ; Liehr, Thomas ; Abdelhay, Eliana ; Silva, Maria Luiza Macedo ; de Souza Fernandez, Teresa

Molecular cytogenetics, 2017, Vol.10, p.35-35

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