Publicaciones en las que colabora con María Currás Freixes (2)
2017
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Targeted sequencing reveals low-frequency variants in EPHA genes as markers of paclitaxel-induced peripheral neuropathy
Clinical Cancer Research, Vol. 23, Núm. 5, pp. 1227-1235
2015
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Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients
Journal of Medical Genetics, Vol. 52, Núm. 10, pp. 647-656