Retinoblastoma and the 13q Deletion Syndrome
Author:
Publisher
SLACK, Inc.
Subject
Ophthalmology,General Medicine,Pediatrics, Perinatology and Child Health
Reference24 articles.
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2. 2. Friend SH Bernards R Rogclj S et al. A human DNA segment with properties of the gene thai predisposes ro retinoblastoma and osteosarcoma. Nature. 1986; 323:643-646.
3. 3. Wadayama B Toguchida J. Shimuzu T. et al. Mutation specttum of the RB gene in osteosatcoma. Cancer Ka. 1994; 54:3042-3048.
4. 4. Lipinski MM Jacks T. The retinoblastoma gene family in dirrerenciation and development. Oncogene. 1999; 18:7873-78 82.
5. 5. Wiggs JL Dryja TR Predicting the risk of hereditary retinoblastomas-AmJOfhthabnal. 1988; 106:346-351.
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1. 13q Deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins;European Journal of Ophthalmology;2012-09
2. Autopsy case of a patient with 13q− syndrome;Legal Medicine;2010-05
3. Brain Abnormalities on MR Imaging in Patients with Retinoblastoma;American Journal of Neuroradiology;2010-04-22
4. Retinoblastoma and deletion of the long arm of chromosome 13: An underestimated diagnosis?;Pediatric Blood & Cancer;2008
5. Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome;Clinical and Experimental Ophthalmology;2004-02
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