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Gabriel Capellá
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Works
5
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients
scientific article published on 30 March 2020
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype
scientific article published on 01 February 2019
Cancer Risks for PMS2-Associated Lynch Syndrome
scientific article published on 30 August 2018
Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes.
scientific article
Detection of APC gene deletions using quantitative multiplex PCR of short fluorescent fragments
scientific article published on 16 May 2008
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Researcher
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