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J Genet Genomics. 2018 Jan 20;45(1):41-45. doi: 10.1016/j.jgg.2017.12.001. Epub 2017 Dec 20.

Rare germline copy number variants in colorectal cancer predisposition characterized by exome sequencing analysis.

Author information

1
Gastroenterology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute, CIBER of Hepatic and Digestive Diseases, University of Barcelona, Barcelona 08036, Spain.
2
Molecular Oncology Laboratory, Hospital Clínico San Carlos, Health Research Institute of the Hospital Clínico San Carlos, Madrid 28040, Spain.
3
Department of Pathology, Hospital Clinic de Barcelona, Barcelona 08036, Spain.
4
Bioinformatics Platform, CIBER of Hepatic and Digestive Diseases, Barcelona 08036, Spain.
5
National Center of Genomic Analysis, Science Park of Barcelona, Barcelona 08028, Spain.
6
Andalusian Developmental Biology Institute, CSIC-Pablo de Olavide University-Andalusian Regional Government, Sevilla 41013, Spain.
7
Gastroenterology Department, Hospital Donostia-Biodonostia Institute, CIBER of Hepatic and Digestive Diseases, University of the Basque Country (UPV/EHU), San Sebastián 20080, Spain.
8
Galician Public Foundation of Genomic Medicine (FPGMX), CIBER of Rare Diseases, Genomics Medicine Group, Hospital Clínico Universitario, University of Santiago de Compostela, Santiago de Compostela 15706, Spain.
9
Gastroenterology Department, Complexo Hospitalario Universitario de Ourense, Ourense Biomedical Research Institute, Ourense 32005, Spain.
10
Gastroenterology Department, Hospital Clínic de Barcelona, August Pi i Sunyer Biomedical Research Institute, CIBER of Hepatic and Digestive Diseases, University of Barcelona, Barcelona 08036, Spain. Electronic address: sbel@clinic.cat.
PMID:
29396139
DOI:
10.1016/j.jgg.2017.12.001
[Indexed for MEDLINE]

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