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Results 1 - 10 of 73  for Great Falls College MSU

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Conference Proceeding
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Positive selection of yeast nonhomologous end-joining genes and a retrotransposon conflict hypothesis

Sawyer , S.L. ; Malik , H.S. 2006

Proceedings of the National Academy of Sciences of the United States of America, 2006, Vol.103, pp.17614-17619 [Peer Reviewed Journal]

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Article
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Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study

Dyment, Da ; Tetreault, M ; Beaulieu, Cl ; Hartley, T ; Ferreira, P ; Chardon, JW ; Marcadier, J ; Sawyer, Sl ; Mosca, SJ ; Innes, Am ; Parboosingh, Js ; Bulman, De ; Schwartzentruber, J ; Majewski, J ; Tarnopolsky, M ; Boycott, Km

Clinical Genetics, Jul 2015, Vol.88(1), pp.34-40 [Peer Reviewed Journal]

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3
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Article
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Negligible validation rate for public domain stop-codon SNPs

Sawyer, Sl ; Berglind, Lc ; Brookes, Aj

Human mutation, 2003, Vol.22(3), pp.252-254 [Peer Reviewed Journal]

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4
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Article
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Scoring insertion-deletion polymorphisms by dynamic allele-specific hybridization

Sawyer, Sl ; Howell, Wm ; Brookes, Aj

BioTechniques, 2003, Vol.35(2), pp.292-+ [Peer Reviewed Journal]

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Article
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Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.(Report)

Sawyer, S. L. ; Hartley, T. ; Dyment, D. A. ; Beaulieu, C. L. ; Schwartzentruber, J. ; Smith, A. ; Bedford, H. M. ; Bernard, G. ; Bernier, F. P. ; Brais, B. ; Bulman, D. E. ; Warman Chardon, J. ; Chitayat, D. ; Deladoey, J. ; Fernandez, B. A. ; Frosk, P. ; Geraghty, M. T. ; Gerull, B. ; Gibson, W. ; Gow, R. M. ; Graham, G. E. ; Green, J. S. ; Heon, E. ; Horvath, G. ; Innes, A. M. ; Jabado, N. ; Kim, R. H. ; Koenekoop, R. K. ; Khan, A. ; Lehmann, O. J. ; Mendoza - Londono, R. ; Michaud, J. L. ; Nikkel, S. M. ; Penney, L. S. ; Polychronakos, C. ; Richer, J. ; Rouleau, G. A. ; Samuels, M. E. ; Siu, V. M. ; Suchowersky, O. ; Tarnopolsky, M. A. ; Yoon, G. ; Zahir, F. R. ; Majewski, J. ; Boycott, K. M.

Clinical Genetics, March, 2016, Vol.89(3), p.275(10) [Peer Reviewed Journal]

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Article
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Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management

Avila, M ; Dyment, Da ; Sagen, Jv ; St-Onge, J ; Moog, U ; Chung, Bhy ; Mo, S ; Mansour, S ; Albanese, A ; Garcia, S ; Martin, Do ; Lopez, AA ; Claudi, T ; Konig, R ; White, SM ; Sawyer, Sl ; Bernstein, Ja ; Slattery, L ; Jobling, Rk ; Yoon

Clinical Genetics, Apr 2016, Vol.89(4), pp.501-506 [Peer Reviewed Journal]

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Article
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Linkage disequilibrium patterns vary substantially among populations

Sawyer, Sl ; Mukherjee, N ; Pakstis, Aj ; Feuk, L ; Kidd, Jr ; Brookes, Aj ; Kidd, Kk

European journal of human genetics : EJHG, 2005, Vol.13(5), pp.677-686 [Peer Reviewed Journal]

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Article
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Haplotype block structures show significant variation among populations

Liu, Nj ; Sawyer, Sl ; Mukherjee, N ; Pakstis, Aj ; Kidd, Jr ; Kidd, Kk ; Brookes, Aj ; Zhao, Hy

Genetic epidemiology, 2004, Vol.27(4), pp.385-400 [Peer Reviewed Journal]

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Article
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Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection

Fredman, D ; Sawyer, Sl ; Stromqvist, L ; Mottagui-Tabar, S ; Kidd, Kk ; Wahlestedt, C ; Chanock, Sj ; Brookes, Aj

Human mutation, 2006, Vol.27(2), pp.173-186 [Peer Reviewed Journal]

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Article
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Lack of replication of association findings in complex disease: An analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease

Prince, J.A. ; Feuk, L. ; Sawyer, S.L. ; Gottfries, J. ; Ricksten, A. ; Nägga, Katarina ; Bogdanovic, N. ; Blennow, K. ; Brookes, A.J. ; Nagga, K

European Journal of Human Genetics, 2001, Vol.9(6), pp.437-444 [Peer Reviewed Journal]

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