Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma

PURPOSE: The availability of molecular genetic testing for retinoblastoma (RB) in Malaysia has enabled patients with a heritable predisposition to the disease to be identified, which thus improves the clinical management of these patients and their families. In this paper, we presented our strategy...

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Detalles Bibliográficos
Autores principales: Mohd Khalid, Mohd Khairul Nizam, Yakob, Yusnita, Md Yasin, Rohani, Wee Teik, Keng, Gaik Siew, Ch’ng, Rahmat, Jamalia, Ramasamy, Sunder, Alagaratnam, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605750/
https://www.ncbi.nlm.nih.gov/pubmed/26539030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605750/
https://www.ncbi.nlm.nih.gov/pubmed/26539030

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