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
一名由范可尼贫血发展而来的骨髓增生异常综合征/急性髓系白血病患儿，携带罕见的t(9;11)(p24;q22)易位，伴有ATM和KMT2A基因的单等位基因缺失。
期刊:Molecular Cytogenetics
影响因子:1.4
doi:10.1186/s13039-018-0389-x
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
