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t(2;18)(p12;q21)

MedGen UID:
272956
Concept ID:
C1515754
Cell or Molecular Dysfunction

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(2;18)(p12;q21)

Recent clinical studies

Diagnosis

Goto H, Sasaki Y, Abe Y, Kon T, Mizumoto N, Yagi M, Sakai T, Ito M, Umehara M, Nakamura S, Tsuchida H, Ueno Y
Clin J Gastroenterol 2022 Feb;15(1):101-106. Epub 2021 Oct 6 doi: 10.1007/s12328-021-01530-3. PMID: 34617259

Therapy

Goto H, Sasaki Y, Abe Y, Kon T, Mizumoto N, Yagi M, Sakai T, Ito M, Umehara M, Nakamura S, Tsuchida H, Ueno Y
Clin J Gastroenterol 2022 Feb;15(1):101-106. Epub 2021 Oct 6 doi: 10.1007/s12328-021-01530-3. PMID: 34617259

Supplemental Content

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