Cargando…
Linkage analysis revealed risk loci on 6p21 and 18p11.2-q11.2 in familial colon and rectal cancer, respectively
Colorectal cancer (CRC) is one of the major cancer types in the western world including Sweden. However, known genetic risk factors could only explain a limited part of heritability of the disease. Moreover, colon and rectal cancers are habitually discussed as one entity, colorectal cancer, although...
Autores principales: | von Holst, Susanna, Jiao, Xiang, Liu, Wen, Kontham, Vinaykumar, Thutkawkorapin, Jessada, Ringdahl, Jenny, Bryant, Patrick, Lindblom, Annika |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6777498/ https://www.ncbi.nlm.nih.gov/pubmed/30952955 http://dx.doi.org/10.1038/s41431-019-0388-3 |
Ejemplares similares
-
Exome sequencing in one family with gastric- and rectal cancer
por: Thutkawkorapin, Jessada, et al.
Publicado: (2016) -
A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31
por: Barnekow, Elin, et al.
Publicado: (2023) -
Linkage Analysis in Familial Non-Lynch Syndrome Colorectal Cancer Families from Sweden
por: Kontham, Vinaykumar, et al.
Publicado: (2013) -
Sensory processing in 16p11.2 deletion and 16p11.2 duplication
por: Smith, Harriet, et al.
Publicado: (2022) -
Two novel colorectal cancer risk loci in the region on chromosome 9q22.32
por: Thutkawkorapin, Jessada, et al.
Publicado: (2018)