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t(1;22)

MedGen UID:
1784929
•Concept ID:
C5446638
•
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that involves a translocation between chromosomes 1 and 22. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;22)

Professional guidelines

PubMed

Virtual simulation of otolith movement for the diagnosis and treatment of benign paroxysmal positional vertigo.
Kong L, Wu J, Feng M, Zhang Y, Liu Z, Yang X
Biomed Tech (Berl) 2021 Aug 26;66(4):387-393. Epub 2021 Feb 11 doi: 10.1515/bmt-2020-0278. PMID: 33567178
White Matter Hyperintensity Accumulation During Treatment of Late-Life Depression.
Khalaf A, Edelman K, Tudorascu D, Andreescu C, Reynolds CF, Aizenstein H
Neuropsychopharmacology 2015 Dec;40(13):3027-35. Epub 2015 Jun 10 doi: 10.1038/npp.2015.158. PMID: 26058663Free PMC Article
Cytogenetic study of acute lymphoblastic leukemia and its correlation with immunophenotype and genotype.
Tien HF, Wang CH, Lee FY, Liu MC, Chuang SM, Chen YC, Shen MC, Lin DT, Lin KH, Chuu WM
Cancer Genet Cytogenet 1992 Apr;59(2):191-8. doi: 10.1016/0165-4608(92)90214-s. PMID: 1581884

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