Published in
BioMed Central, Molecular Cytogenetics, 1(11), 2018
DOI: 10.1186/s13039-018-0389-x
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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
Journal article published in 2018 by
Viviane Lamim Lovatel 
,
Daiane Corrêa de Souza,
Tatiana Fonseca Alvarenga,
Roberto R. Capela de Matos,
Claudia Diniz,
Marcia Trindade Schramm,
Juan Clinton Llerena Júnior,
Maria Luiza Macedo Silva,
Eliana Abdelhay,
Teresa de Souza Fernandez
,
Daiane Corrêa de Souza,
Tatiana Fonseca Alvarenga,
Roberto R. Capela de Matos,
Claudia Diniz,
Marcia Trindade Schramm,
Juan Clinton Llerena Júnior,
Maria Luiza Macedo Silva,
Eliana Abdelhay,
Teresa de Souza Fernandez
This paper is made freely available by the publisher.
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