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t(3;14)(p14.1;q32)

MedGen UID:
318462
Concept ID:
C1711150
Cell or Molecular Dysfunction

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(3;14)(p14.1;q32)

Recent clinical studies

Diagnosis

Sasaki Y, Shiozawa E, Watanabe N, Homma M, Noh JY, Ito K, Takimoto M, Yamochi-Onizuka T
Leuk Res 2020 Aug;95:106399. Epub 2020 Jun 2 doi: 10.1016/j.leukres.2020.106399. PMID: 32534365

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    Practice guidelines

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