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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2009
Teme:
Case Report
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2758865/
https://ncbi.nlm.nih.gov/pubmed/19772601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-10-97
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items