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Hypertension (Dallas, Tex. : 1979)|October 20, 2001
Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4pH Allayee, T W de Bruin, K Michelle Dominguez, et al.Gut|October 4, 2008
Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activationH Takedatsu, K D Taylor, L Mei, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 1, 1996
Helicobacter pylori antibodies in relation to precancerous gastric lesions in a high-risk Chinese populationL Zhang, W J Blot, W C You, et al.The Journal of Clinical Investigation|April 20, 1999
PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosusB P Tsao, R M Cantor, J M Grossman, et al.Circulation|January 4, 2001
Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive probandA H Xiang, S P Azen, L J Raffel, et al.Human Molecular Genetics|October 1, 1996
Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitisJ D Ohmen, H Y Yang, K K Yamamoto, et al.Diabetologia|March 16, 2013
Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearanceM O Goodarzi, X Guo, J Cui, et al.European Journal of Human Genetics : EJHG|May 11, 1999
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosisM Shohat, N Magal, T Shohat, et al.International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 11, 2000
Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1AC J van der Kallen, R M Cantor, M M van Greevenbroek, et al.American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.Pageof 42