Two novel colorectal cancer risk loci in the region on chromosome 9q22.32

Highly penetrant cancer syndromes account for less than 5% of all cases with familial colorectal cancer (CRC), and other genetic contribution explains the majority of the genetic contribution to CRC. A CRC susceptibility locus on chromosome 9q has been suggested. In this study, families where risk o...

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Dades bibliogràfiques
Publicat a:Oncotarget
Autors principals: Thutkawkorapin, Jessada, Mahdessian, Hovsep, Barber, Tom, Picelli, Simone, von Holst, Susanna, Lundin, Johanna, Valle, Laura, Kontham, Vinaykumar, Liu, Tao, Nilsson, Daniel, Jiao, Xiang, Lindblom, Annika
Format: Artigo
Idioma:Inglês
Publicat: Impact Journals LLC 2018
Matèries:
Research Paper
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5834248/
https://ncbi.nlm.nih.gov/pubmed/29541405
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.24340
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