Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features-Reference-Cited by-同舟云学术

Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features

Published:2020-06 Issue:6 Volume:127 Page:804-813
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Afshar Armin R.,Pekmezci Melike,Bloomer Michele M.,Cadenas Nicola J.,Stevers Meredith,Banerjee Anuradha,Roy Ritu,Olshen Adam B.,Van Ziffle Jessica,Onodera Courtney^ORCID,Devine W. Patrick,Grenert James P.,Bastian Boris C.,Solomon David A.^ORCID,Damato Bertil E.

Funder

Research to Prevent Blindness

National Eye Institute

National Institutes of Health

Publisher

Elsevier BV

Subject

Ophthalmology

Reference25 articles.

1. Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes;Kooi;Sci Rep,2016

2. Frequency of somatic and germ-line mosaicism in retinoblastoma: implications for genetic counseling;Sippel;Am J Human Genet,1998

3. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing;Chen;Hum Mutat,2014