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Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies.
Pearson JV, Huentelman MJ, Halperin RF, Tembe WD, Melquist S, Homer N, Brun M, Szelinger S, Coon KD, Zismann VL, Webster JA, Beach T, Sando SB, Aasly JO, Heun R, Jessen F, Kolsch H, Tsolaki M, Daniilidou M, Reiman EM, Papassotiropoulos A, Hutton ML, Stephan DA, Craig DW. Pearson JV, et al. Among authors: kolsch h. Am J Hum Genet. 2007 Jan;80(1):126-39. doi: 10.1086/510686. Epub 2006 Dec 6. Am J Hum Genet. 2007. PMID: 17160900 Free PMC article.
Lack of genetic dispositions to hyperhomocysteinemia in Alzheimer disease.
Linnebank M, Linnebank A, Jeub M, Klockgether T, Wüllner U, Kölsch H, Heun R, Koch HG, Suormala T, Fowler B. Linnebank M, et al. Among authors: kolsch h. Am J Med Genet A. 2004 Nov 15;131(1):101-2. doi: 10.1002/ajmg.a.30295. Am J Med Genet A. 2004. PMID: 15389705 No abstract available.
130 results