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Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.
Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA. Bétard C, et al. Among authors: chagnon p. Am J Hum Genet. 2000 Jul;67(1):222-8. doi: 10.1086/302993. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820129 Free PMC article.
Identification and characterization of an Xp22.33;Yp11.2 translocation causing a triplication of several genes of the pseudoautosomal region 1 in an XX male patient with severe systemic lupus erythematosus.
Chagnon P, Schneider R, Hébert J, Fortin PR, Provost S, Belisle C, Gingras M, Bolduc V, Perreault C, Silverman E, Busque L. Chagnon P, et al. Arthritis Rheum. 2006 Apr;54(4):1270-8. doi: 10.1002/art.21733. Arthritis Rheum. 2006. PMID: 16575839 Free article.
Specific pathological Tau protein variants characterize Pick's disease.
Delacourte A, Robitaille Y, Sergeant N, Buée L, Hof PR, Wattez A, Laroche-Cholette A, Mathieu J, Chagnon P, Gauvreau D. Delacourte A, et al. Among authors: chagnon p. J Neuropathol Exp Neurol. 1996 Feb;55(2):159-68. doi: 10.1097/00005072-199602000-00004. J Neuropathol Exp Neurol. 1996. PMID: 8786374
46 results