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t(7;12)(q36;p13)

MedGen UID:
885829
Concept ID:
C4053813
Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the ETV6 gene on chromosome 12p13 and HLXB9 gene on chromosome 7q36. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(7;12)(q36;p13)

Professional guidelines

PubMed

Ragusa D, Dijkhuis L, Pina C, Tosi S
Biosci Rep 2023 Jan 31;43(1) doi: 10.1042/BSR20220489. PMID: 36622782Free PMC Article

Recent clinical studies

Diagnosis

Espersen ADL, Noren-Nyström U, Abrahamsson J, Ha SY, Pronk CJ, Jahnukainen K, Jónsson ÓG, Lausen B, Palle J, Zeller B, Palmqvist L, Hasle H
Genes Chromosomes Cancer 2018 Jul;57(7):359-365. Epub 2018 Apr 30 doi: 10.1002/gcc.22538. PMID: 29569294

Prognosis

Espersen ADL, Noren-Nyström U, Abrahamsson J, Ha SY, Pronk CJ, Jahnukainen K, Jónsson ÓG, Lausen B, Palle J, Zeller B, Palmqvist L, Hasle H
Genes Chromosomes Cancer 2018 Jul;57(7):359-365. Epub 2018 Apr 30 doi: 10.1002/gcc.22538. PMID: 29569294

Supplemental Content

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