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inv(22)

MedGen UID:
273724
•Concept ID:
C1515663
•
Cell or Molecular Dysfunction

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVinv(22)

Professional guidelines

PubMed

Modern molecular diagnostics and the management of haematological malignancies.
Morgan GJ, Pratt G
Clin Lab Haematol 1998 Jun;20(3):135-41. doi: 10.1046/j.1365-2257.1998.00141.x. PMID: 9681227

Recent clinical studies

Etiology

Study of intron 22 inversion mutation in north India with review.
Kumar P, Faridi NJ, Husain N, Soni P, Goel SK
Blood Coagul Fibrinolysis 2013 Mar;24(2):120-4. doi: 10.1097/MBC.0b013e3283574f40. PMID: 23322272

Diagnosis

A strategy for the molecular diagnosis in hemophilia a in Chinese population.
He Z, Chen J, Xu S, Chen S, Xiao X, Li H, Guo Y, Jiang W
Cell Biochem Biophys 2013 Apr;65(3):463-72. doi: 10.1007/s12013-012-9450-2. PMID: 23111982

Clinical prediction guides

Identification of six novel factor viii gene variants using next generation sequencing and molecular dynamics simulation.
Al-Allaf FA, Abduljaleel Z, Bogari NM, Owaidah TMA, Taher MM, Athar M, Elsendiony A, Abalkhail H, Abdellatif A, Elbjeirami W, Bouazzaoui A
Acta Biochim Pol 2019 Feb 22;66(1):23-31. doi: 10.18388/abp.2018_2339. PMID: 30793713
Study of intron 22 inversion mutation in north India with review.
Kumar P, Faridi NJ, Husain N, Soni P, Goel SK
Blood Coagul Fibrinolysis 2013 Mar;24(2):120-4. doi: 10.1097/MBC.0b013e3283574f40. PMID: 23322272

Supplemental Content

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    Practice guidelines

    • PubMed
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