2018
Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion.
Shah S, Koban Y, Le BHA, Bechtold M, Zolfaghari E, Kim JW, Berry JL. Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion. Journal Of Pediatric Ophthalmology & Strabismus 2018, 55: e10-e13. PMID: 29684226, PMCID: PMC7444716, DOI: 10.3928/01913913-20180215-02.Peer-Reviewed Original ResearchChromosome DeletionChromosome DisordersChromosomes, Human, Pair 13Diagnosis, DifferentialDNA Mutational AnalysisDNA, NeoplasmFemaleFluorescein AngiographyFundus OculiHumansInfantIrisIris DiseasesMagnetic Resonance ImagingMutationPigmentation DisordersRetinoblastomaRetinoblastoma Binding ProteinsTomography, Optical CoherenceUbiquitin-Protein Ligases
2017
Lack of correlation between age at diagnosis and RB1 mutations for unilateral retinoblastoma: the importance of genetic testing
Berry JL, Lewis L, Zolfaghari E, Green S, Le BHA, Lee TC, Murphree AL, Kim JW, Jubran R. Lack of correlation between age at diagnosis and RB1 mutations for unilateral retinoblastoma: the importance of genetic testing. Ophthalmic Genetics 2017, 39: 408-410. PMID: 29286867, PMCID: PMC7446179, DOI: 10.1080/13816810.2017.1420807.Peer-Reviewed Original Research