The RB1 gene mutation in a child with ectopic intracranial retinoblastoma.

Eitemau Tebyg

• Ectopic intracranial retinoblastoma in childhood.
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• Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 gene.
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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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  Cyhoeddwyd: (1992)
• Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
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• Spectrum of mutations in the RB1 gene in Vietnamese patients with retinoblastoma
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  Cyhoeddwyd: (2019-04-01)