Spectrum of gross deletions and insertions in theRB1 gene in patients with retinoblastoma and association with phenotypic expression
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference42 articles.
1. Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B element
2. Stress-induced duplex DNA destabilization in scaffold/matrix attachment regions
3. Molecular detection of constitutional deletions in patients with retinoblastoma
4. Deletion of RBExons 24 and 25 Causes Low-Penetrance Retinoblastoma
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