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

Benzer Materyaller

• Co-deleting Pten with Rb in retinal progenitor cells in mice results in fully penetrant bilateral retinoblastomas
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• 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
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• Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.
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  Baskı/Yayın Bilgisi: (1992)
• Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
  Yazar:: Shimizu, T., ve diğerleri
  Baskı/Yayın Bilgisi: (1994)
• Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB function
  Yazar:: Otterson, Gregory A., ve diğerleri
  Baskı/Yayın Bilgisi: (1997)