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Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma

PURPOSE: Retinoblastoma (RB), the most common intraocular tumor occurring in infancy and early childhood, is most often related to mutations in the RB1 gene. In this study, we screened the RB1 germline mutations in 41 unrelated Moroccan patients with retinoblastoma, 25 heritable cases, and 16 sporad...

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Detalhes bibliográficos
Main Authors: Abidi, Omar, Knari, Sara, Sefri, Hajar, Charif, Majida, Senechal, Audrey, Hamel, Christian, Rouba, Hassan, Zaghloul, Khalid, El Kettani, Asmaa, Lenaers, Guy, Barakat, Abdelhamid
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3250372/
https://ncbi.nlm.nih.gov/pubmed/22219649
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