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Article

A Rare Case of ETV6/MECOM Rearrangement in Therapy-Related Acute Myeloid Leukemia with t(3;12) and Monosomy 7.

Clinical laboratory - 1 Feb 2017

Kim Young Jin, Yang John J, Han Yujin, Kim Suekyeung, Yang Hyung-Seok, Yoon Hwi-Joong, Lee Ju Hie, Lee Woo-In, Park Tae Sung

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Share to Chromosomes, Human, Pair 12
Share to Chromosomes, Human, Pair 3
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to ETS Translocation Variant 6 Protein

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Identifiers

PMID: 28182364
DOI: 10.7754/Clin.Lab.2016.160815

Genes

ETV6
MECOM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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A Rare Case of ETV6/MECOM Rearrangement in Therapy-Related Acute Myeloid Leukemia with t(3;12) and Monosomy 7.PMID 28182364Read ↗

A rare case of acute myeloid leukemia with a CHIC2-ETV6 fusiongen and multiple other molecular aberrations.Semantic proximity Read ↗

<i>ETV6</i> rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic eventsSemantic proximity Read ↗

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Myeloproliferative neoplasm with ETV6-ABL1 fusion: a case report and literature reviewSemantic proximity Read ↗

ETV6-NTRK3 is Associated With Trisomy 8 and Sensitive to TRK Inhibitor in Hematologic Malignancy: Case Report of a Refractory AML and Review of the LiteratureSemantic proximity Read ↗

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FLT3 is fused to ETV6 in a myeloproliferative disorder with hypereosinophilia and a t(12;13)(p13;q12) translocationSemantic proximity Read ↗

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