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Page 1
Cardiomyopathy in congenital complete lipodystrophy.
Bhayana S, Siu VM, Joubert GI, Clarson CL, Cao H, Hegele RA. Bhayana S, et al. Among authors: siu vm. Clin Genet. 2002 Apr;61(4):283-7. doi: 10.1034/j.1399-0004.2002.610407.x. Clin Genet. 2002. PMID: 12030893
A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems.
Lahiry P, Wang J, Robinson JF, Turowec JP, Litchfield DW, Lanktree MB, Gloor GB, Puffenberger EG, Strauss KA, Martens MB, Ramsay DA, Rupar CA, Siu V, Hegele RA. Lahiry P, et al. Am J Hum Genet. 2009 Feb;84(2):134-47. doi: 10.1016/j.ajhg.2008.12.017. Epub 2009 Jan 29. Am J Hum Genet. 2009. PMID: 19185282 Free PMC article.
Amish, mennonite, and hutterite genetic disorder database.
Payne M, Rupar CA, Siu GM, Siu VM. Payne M, et al. Among authors: siu vm, siu gm. Paediatr Child Health. 2011 Mar;16(3):e23-4. doi: 10.1093/pch/16.3.e23. Paediatr Child Health. 2011. PMID: 22379385 Free PMC article. No abstract available.
A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America.
Loucks C, Parboosingh JS, Chong JX, Ober C, Siu VM, Hegele RA, Rupar CA, McLeod DR, Pinto A, Chudley AE, Innes AM. Loucks C, et al. Among authors: siu vm. Am J Med Genet A. 2012 May;158A(5):1229-32. doi: 10.1002/ajmg.a.35302. Epub 2012 Apr 11. Am J Med Genet A. 2012. PMID: 22495976 Free PMC article. No abstract available.
98 results