Pathogenesis of vestibular schwannoma in ring chromosome 22

BACKGROUND: Ring chromosome 22 is a rare human constitutional cytogenetic abnormality. Clinical features of neurofibromatosis type 1 and 2 as well as different tumour types have been reported in patients with ring chromosome 22. The pathogenesis of these tumours is not always clear yet. METHODS: We...

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Detalles Bibliográficos
Autores principales: Denayer, Ellen, Brems, Hilde, de Cock, Paul, Evans, Gareth D, Van Calenbergh, Frank, Bowers, Naomi, Sciot, Raf, Debiec-Rychter, Maria, Vermeesch, Joris V, Fryns, Jean-Pierre, Legius, Eric
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758865/
https://www.ncbi.nlm.nih.gov/pubmed/19772601
http://dx.doi.org/10.1186/1471-2350-10-97

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758865/
https://www.ncbi.nlm.nih.gov/pubmed/19772601
http://dx.doi.org/10.1186/1471-2350-10-97

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