E. Hernández-Imaz

Monozygotic twins with Neurofibromatosis type 1, concordant phenotype and synchronous development of MPNST and metastasis

M. C. Valero, C. Hernández-Chico, Y. Martín, 2010, BMC Cancer.

RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas

C. Hernández-Chico, Y. Martín, G. Meleán, 2012, neurogenetics.

Characterization of NF1 allele containing two nonsense mutations in exon 37 that segregates with neurofibromatosis type 1

C. Hernández-Chico, Y. Martín, B. Campos, 2013, Clinical genetics.

A highly sensitive genetic protocol to detect NF1 mutations.

M. C. Valero, C. Hernández-Chico, D. Tellería, 2011, The Journal of molecular diagnostics : JMD.

Functional Analysis of Mutations in Exon 9 of NF1 Reveals the Presence of Several Elements Regulating Splicing

Marco Baralle, M. Baralle, L. De Conti, 2015, PloS one.

RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas

Y. Martín, G. Meleán, E. Hernández-Imaz, 2012, Neurogenetics.