Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum

Por Caglayan, AO, Per, H, Akgumus, G, Gumus, H, Baranoski, J, Canpolat, M, Calik, M, Yikilmaz, A, Bilguvar, K, Kumandas, S, Gunel, M
Publicado em 2013

P12.06 Significantly Mutated Genes for Radiation-Associated Meningioma

Por Claus, E. B., Greenhalgh, S., Gaffney, S. G., Bilguvar, K., Calvocoressi, L., Lu, L., Al-Mefty, O., Zi-Ming Zhao, Z., Townsend, J. P.
Publicado no Neuro Oncol (2017)