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Roberto R. Capela de Matos
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Roberto R. Capela de Matos
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Roberto R. Capela de Matos
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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
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
Published 2018-07-01
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