VICTOR MANUEL
BARBERA JUAN
PROFESOR/A ASOCIADO/A LOU
Hospital Universitario La Fe
Valencia, EspañaPublikationen in Zusammenarbeit mit Forschern von Hospital Universitario La Fe (6)
2019
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Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes: Diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)
Hereditary Cancer in Clinical Practice, Vol. 17, Núm. 1
2017
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Characterization of a novel POLD1 missense founder mutation in a Spanish population
Journal of Gene Medicine, Vol. 19, Núm. 4
2014
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Prevalence of germline MUTYH mutations among Lynch-like syndrome patients
European Journal of Cancer, Vol. 50, Núm. 13, pp. 2241-2250
2012
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Recurrent testicular germ cell tumors in a family with MYH-Associated polyposis
Journal of Clinical Oncology, Vol. 30, Núm. 23
2011
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Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome
BMC Medical Genetics, Vol. 12
2010
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EPCAM germ line deletions as causes of lynch syndrome in Spanish patients
Journal of Molecular Diagnostics, Vol. 12, Núm. 6, pp. 765-770