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589 results
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Structural variation in the human genome.
Feuk L, Carson AR, Scherer SW. Feuk L, et al. Among authors: scherer sw. Nat Rev Genet. 2006 Feb;7(2):85-97. doi: 10.1038/nrg1767. Nat Rev Genet. 2006. PMID: 16418744 Review.
Resources for human genetics on the World Wide Web.
Osborne LR, Lee JR, Scherer SW. Osborne LR, et al. Among authors: scherer sw. Mol Med Today. 1997 Sep;3(9):370-3. doi: 10.1016/S1357-4310(97)82918-8. Mol Med Today. 1997. PMID: 9302686
Genome analysis.
Scherer SW, Hoheisel JD. Scherer SW, et al. Mol Med Today. 1995 Sep;1(6):258-9. doi: 10.1016/s1357-4310(95)90999-0. Mol Med Today. 1995. PMID: 9415159 No abstract available.
Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.
Nakabayashi K, Fernandez BA, Teshima I, Shuman C, Proud VK, Curry CJ, Chitayat D, Grebe T, Ming J, Oshimura M, Meguro M, Mitsuya K, Deb-Rinker P, Herbrick JA, Weksberg R, Scherer SW. Nakabayashi K, et al. Among authors: scherer sw. Genomics. 2002 Feb;79(2):186-96. doi: 10.1006/geno.2002.6695. Genomics. 2002. PMID: 11829489
Mutations in SUFU predispose to medulloblastoma.
Taylor MD, Liu L, Raffel C, Hui CC, Mainprize TG, Zhang X, Agatep R, Chiappa S, Gao L, Lowrance A, Hao A, Goldstein AM, Stavrou T, Scherer SW, Dura WT, Wainwright B, Squire JA, Rutka JT, Hogg D. Taylor MD, et al. Among authors: scherer sw. Nat Genet. 2002 Jul;31(3):306-10. doi: 10.1038/ng916. Epub 2002 Jun 17. Nat Genet. 2002. PMID: 12068298
Genetic analysis of patients with the Saethre-Chotzen phenotype.
Chun K, Teebi AS, Jung JH, Kennedy S, Laframboise R, Meschino WS, Nakabayashi K, Scherer SW, Ray PN, Teshima I. Chun K, et al. Among authors: scherer sw. Am J Med Genet. 2002 Jun 15;110(2):136-43. doi: 10.1002/ajmg.10400. Am J Med Genet. 2002. PMID: 12116251
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