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Disease: Chromosome 8- monosomy 8p2

  • Deletion of Chromosomal Region 8p21 Confers Resistance to Bortezomib and Is Associated with Upregulated Decoy TRAIL Receptor Expression in Patients with Multiple Myeloma
  • Early immune reconstitution and efficient graft vs tumor effect after unrelated partially matched double cord blood transplantation in refractory 8p11 syndrome
  • Genomic profile of copy number variants on the short arm of human chromosome 8
  • Hepatitis B virus infection is associated with deletion of chromosome 8p in multiple myeloma
  • Mouse model implicates GNB3 duplication in a childhood obesity syndrome
  • Prenatal diagnosis of inverted duplication deletion 8p syndrome mimicking trisomy 18
  • Submicroscopic deletion of FGFR1 gene is recurrently detected in myeloid and lymphoid neoplasms associated with ZMYM2-FGFR1 rearrangements: a case study
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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