REFERENCES
- Abramson DH, Mendelsohn ME, Servodidio CA, Tretter T, Gombos DS. Familial retinoblastoma: where and when? Acta Ophthalmol Scand 1998;76:334–338.
- Connolly MJ, Payne RH, Johnson G et al. Familial, EsD-linked, retinoblastoma with reduced penetrance and variable expressivity. Hum Genet 1983;65:122–124.
- Blach LE, McCormik B, Abramson DH, Ellsworth RM. Trilateral retinoblastoma--incidence and outcome: a decade of experience. Int J Radiat Oncol Biol Phys 1994;29:729–733.
- Shields CL, Mashayekhi A, Carter J et al. Chemoreduction for retinoblastoma. Analysis of tumor control and risks for recurrence in 457 tumors. Am J Ophthalmol 2004;138:329–337.
- Leiderman YI, Kiss S, Mukai S. Molecular genetics of RB1–the retinoblastoma gene. Semin Ophthalmol 2007;22:247–254.
- Harbour JW. Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening. Ophthalmol 1998;105;1442–1447.
- Kajii T, Tsukahara M, Fukushima Y et al. Translocation (X;13)(p11.21;q12.3) in a girl with incontinentia pigmenti and bilateral retinoblastoma. Ann Genet 1985;28:219–223.
- Blanquet V, Turleau C, Créau-Goldberg N et al. De novo t(2;13)(p24.3;q14.2) and retinoblastoma. Mapping of two 13q14 probes by in situ hibridization. Hum Genet 1987;76:102–105.
- Janson M, Nordenskjöld JM. A constitutional mutation within the retinoblastoma gene detected by PFGE. Clin Genet 1994;45:5–10.
- Keith CG, Webb GC. Retinoblastoma and retinoma ocurring in a child with a translocation and deletion of the long arm of chromosome 13. Arch Ophthalmol 1985;103:941–944.
- Cross HE, Hansen RC, AMorrow G 3rd, Davis JR. Retinoblastoma in a patient with a 13qXp translocation. Am J Ophthalmol 1977;84:548–554.
- Triviño E, Guitart M, Egozcue J, Coll MD. Characterization by FISH of a t(5;13) in a patient with bilateral retinoblastoma. Cancer Genet Cytogenet 1997;96:23–25.
- Cowell JK, Hogg A. Genetics and cytogenetics of retinoblastoma. Cancer Genet Cytogenet 1992;64:1–11.
- Kivela T. Trilateral retinoblastoma: a meta-analysis of hereditary retinoblastoma associated with primary ectopic intracranial retinoblastoma. J Clin Oncol 1999;17:1829–1837.
- Valverde JR, Alonso J, Palacios I, Pestaña A. RB1 gene mutation up-date, a meta-analysis based on 932 reported mutations available in a searchable database. BMC Genet 2005;6:53.
- Taylor M, Dehainault C, Desjardins L et al. Genotype-phenotype correlations in hereditary familial retinoblastoma. Hum Mutat 2007;28:284–293.
- Bejjani GK, Donahue DJ, Selby D, Cogen PH, Packer R. Association of a suprasellar mass and intraocular retinoblastoma: a variant of pineal trilateral retinoblastoma? Pediatr Neurosurg 1996;25:269–275.