Constitutional retinoblastoma gene deletion in Egyptian patients-Reference-Cited by-同舟云学术

Constitutional retinoblastoma gene deletion in Egyptian patients

Published:2009-08 Issue:3 Volume:5 Page:222-225
ISSN:1708-8569
Container-title:World Journal of Pediatrics
language:en
Short-container-title:World J Pediatr

Author:

Mohammed Amal M.,Kamel Alaa K.,Hammad Saida A.,Afifi Hanan H.,El Sanabary Zeinab,El Din Mostafa Ezz

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s12519-009-0042-1.pdf

Reference19 articles.

1. OMIM. Online Mendelian Inheritance in Man. 2008, Center for Medical Genetics, John Hopkins University (Baltimore, M.D.) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD). http://www.ncbi.nlm.nih.gov/OMIM (accessed September 3, 2008)

2. Castillo B, Kaufman L. Pediatric tumors of the eye and orbit. Pediatr Clin North Am 2003;50:149–172.

3. Melamud A, Palekar R, Singh A. Retinoblastoma. Am Fam Physician 2006;73:1039–1044.

4. Balmer A, Zografos L, Munier F. Diagnosis and current management of retinoblastoma. Oncogene 2006;25:5341–5349.

5. Medical Encyclopedia, 2008. http://www.answers.com/topic/retinoblastoma (accessed September 3, 2008).

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