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

Molecular Cytogenetics - United Kingdom
doi 10.1186/s13039-018-0389-x
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Springer Science and Business Media LLC

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