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Autor:
Valenzuela I; Department of Clinical and Molecular Genetics and Rare Disease Unit, University Hospital Vall d´Hebron, Barcelona, Spain. Electronic address: mvalenzuela@vhebron.net., Segura-Puimedon M; Quantitative Genomic Medicine Laboratories, Ltd (qGenomics), Esplugues del Llobregat, Catalonia, Spain., Rodríguez-Santiago B; Quantitative Genomic Medicine Laboratories, Ltd (qGenomics), Esplugues del Llobregat, Catalonia, Spain., Fernández-Alvarez P; Department of Clinical and Molecular Genetics and Rare Disease Unit, University Hospital Vall d´Hebron, Barcelona, Spain., Vendrell T; Department of Clinical and Molecular Genetics and Rare Disease Unit, University Hospital Vall d´Hebron, Barcelona, Spain., Armengol L; Quantitative Genomic Medicine Laboratories, Ltd (qGenomics), Esplugues del Llobregat, Catalonia, Spain., Tizzano E; Department of Clinical and Molecular Genetics and Rare Disease Unit, University Hospital Vall d´Hebron, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Barcelona, Spain. Electronic address: etizzano@vhebron.net.
Publikováno v:
European journal of medical genetics [Eur J Med Genet] 2019 Mar; Vol. 62 (3), pp. 182-185. Date of Electronic Publication: 2018 Jul 10.