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Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomas
Neurofibromatosis Type 1 (NF1) is one of the most common autosomal dominant cancer syndromes worldwide. Individuals with NF1 have a wide variety of clinical features including a strongly increased risk for pediatric brain tumors. The etiology of pediatric brain tumor development in NF1 is largely un...
Tallennettuna:
| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2012
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3693850/ https://ncbi.nlm.nih.gov/pubmed/22829012 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10689-012-9549-z |
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