Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma.

Lignende værker

• Co-deleting Pten with Rb in retinal progenitor cells in mice results in fully penetrant bilateral retinoblastomas
  af: Xie, Chencheng, et al.
  Udgivet: (2015)
• A T to C mutation in the polypyrimidine tract of the exon 9 splicing site of the RB1 gene responsible for low penetrance hereditary retinoblastoma
  af: Lefevre, S, et al.
  Udgivet: (2002)
• Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.
  af: Onadim, Z, et al.
  Udgivet: (1992)
• Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
  af: Shimizu, T., et al.
  Udgivet: (1994)
• Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB function
  af: Otterson, Gregory A., et al.
  Udgivet: (1997)