A comprehensive, sensitive and economical approach for the detection of mutations in the RB1 gene in retinoblastoma
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1007/s12041-009-0069-z.pdf
Reference29 articles.
1. Alonso J., Garcia-Miguel P., Abelairas J., Mendiola M., Sarret E., Vendrell M. T. et al. 2001 Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications. Hum. Mutat. 17, 412–422.
2. Ata-ur-Rasheed M., Vemuganti G., Honavar S., Ahmed N., Hasnain S. and Kannabiran C. 2002 Mutational analysis of the RB1 gene in Indian patients with retinoblastoma. Ophthalmic Genet. 23, 121–128.
3. Bamne M. N., Ghule P. N., Jose J., Banavali S.D., Kurkure P.A. and Amare Kadam P. S. 2005 Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India. Genet. Test 9, 200–211.
4. Blanquet V., Turleau C., Gross-Morand M. S., Senamaud-Beaufort C., Doz F. and Besmond C. 1995 Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma. Hum. Mol. Genet. 4, 383–388.
5. Brichard B., Heusterspreute M., De Potter P., Chantrain C., Vermylen C., Sibille C. and Gala J. L. 2006 Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation. Eur. J. Cancer 42, 65–72.
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