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  5. Chromosome 11p- partial deletion

Chromosome 11p- partial deletion

December 31, 2014

Latest Research

  • 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia
  • 50 Years Ago in TheJournalofPediatrics: Understanding the Molecular Basis of 11p13 Deletion
  • A familial pericentric inversion of chromosome 11 associated with a microdeletion of 163 kb and microduplication of 288 kb at 11p13 and 11q22.3 without aniridia or eye anomalies
  • A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)
  • A nude mouse Wilms' tumor line (KCMC-WT-1) derived from an aniridia patient with monoalleleic partial deletion of chromosome 11p
More Research
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