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Spinal neurofibromatosis associated with classical neurofibromatosis type 1: genetic characterisation of an atypical case
Spinal tumours are observed in about 40% of neurofibromatosis type 1 (NF1) patients and occur within two subgroups: (1) NF1 patients carrying classical diagnostic criteria and only one or few spinal tumours and (2) patients with few NF1 stigmata but multiple bilateral spinal tumours, an entity calle...
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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BMJ Publishing Group
2013
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3604550/ https://ncbi.nlm.nih.gov/pubmed/23417386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2012-008468 |
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