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Genes and Immunity|March 12, 2004
Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patientsM J van Belzen, B P C Koeleman, J B A Crusius, et al.Neurogastroenterology and Motility|July 18, 2017
Habitual diet and diet quality in Irritable Bowel Syndrome: A case-control studyE F Tigchelaar, Z Mujagic, A Zhernakova, et al.Human Molecular Genetics|November 7, 2000
Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinantR S Hansen, R Stöger, C Wijmenga, et al.Alimentary Pharmacology & Therapeutics|May 3, 2016
Volatile organic compounds in breath as markers for irritable bowel syndrome: a metabolomic approachA Baranska, Z Mujagic, A Smolinska, et al.European Journal of Human Genetics : EJHG|September 27, 2003
Anticipation in familial intracranial aneurysms in consecutive generationsP M Struycken, G Pals, M Limburg, et al.Gut|November 9, 2007
Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisM C Wapenaar, A J Monsuur, A A van Bodegraven, et al.Human Molecular Genetics|February 9, 1999
Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16B J van de Sluis, M Breen, M Nanji, et al.Gut|January 21, 2006
Lack of association of MYO9B genetic variants with coeliac disease in a British cohortK A Hunt, A J Monsuur, W L McArdle, et al.Animal Genetics|November 19, 2005
Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriersO P Forman, M E G Boursnell, B J Dunmore, et al.Gut Microbes|July 27, 2021
A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel diseaseR Gacesa, A Vich Vila, V Collij, et al.Pageof 12