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Paper Details

Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
BMC Med Genet
13
2016
119 kb duplication, 134 kb large duplication, 15, 7p22, 8q24, ABCC4, CCZ1, CLDN10, CNV, CNV regions, CNVs, KCNK9 gene, OCM, RNF216, SNP, UC, Ulcerative colitis, ZNF815, copy number variants, copy number variations, deleted region, inflammatory bowel disease, patients, polygenic disorder, rare CNV, rare copy number variants, rare genetic variants, susceptibility loci, ulcerative colitis
Author NameAffiliation
Michael WittigInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel
Ingo HelbigUniversity Clinic Schleswig-Holstein
Carl A AndersonWellcome Trust Sanger Institute
Christopher G MathewKing's College London School of Medicine
Philip RosenstielInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel
Stefan SchreiberInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel
Stefan SchreiberUniversity Hospital Schleswig-Holstein
Andre FrankeInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel
Andre FrankeInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel
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