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Page 1
The DNA sequence of the human X chromosome.
Nature. 2005 Mar 17;434(7031):325-37. doi: 10.1038/nature03440.
Nature. 2005.
PMID: 15772651
Free PMC article.
11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity.
Shinawi M, Sahoo T, Maranda B, Skinner SA, Skinner C, Chinault C, Zascavage R, Peters SU, Patel A, Stevenson RE, Beaudet AL.
Shinawi M, et al. Among authors: chinault c.
Am J Med Genet A. 2011 Jun;155A(6):1272-80. doi: 10.1002/ajmg.a.33878. Epub 2011 May 12.
Am J Med Genet A. 2011.
PMID: 21567907
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The complete genome of an individual by massively parallel DNA sequencing.
Wheeler DA, Srinivasan M, Egholm M, Shen Y, Chen L, McGuire A, He W, Chen YJ, Makhijani V, Roth GT, Gomes X, Tartaro K, Niazi F, Turcotte CL, Irzyk GP, Lupski JR, Chinault C, Song XZ, Liu Y, Yuan Y, Nazareth L, Qin X, Muzny DM, Margulies M, Weinstock GM, Gibbs RA, Rothberg JM.
Wheeler DA, et al. Among authors: chinault c.
Nature. 2008 Apr 17;452(7189):872-6. doi: 10.1038/nature06884.
Nature. 2008.
PMID: 18421352
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Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.
Ayyagari R, Nestorowicz A, Li Y, Chandrasekharappa S, Chinault C, van Tuinen P, Smith RJ, Hejtmancik JF, Permutt MA.
Ayyagari R, et al. Among authors: chinault c.
Genome Res. 1996 Jun;6(6):504-14. doi: 10.1101/gr.6.6.504.
Genome Res. 1996.
PMID: 8828039
Free article.
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15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.
Brunetti-Pierri N, Sahoo T, Frioux S, Chinault C, Zascavage R, Cheung SW, Peters S, Shinawi M.
Brunetti-Pierri N, et al. Among authors: chinault c.
Am J Med Genet A. 2008 Aug 1;146A(15):1933-41. doi: 10.1002/ajmg.a.32324.
Am J Med Genet A. 2008.
PMID: 18561338
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Interstitial deletion of 6q25.2-q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss.
Nagamani SC, Erez A, Eng C, Ou Z, Chinault C, Workman L, Coldwell J, Stankiewicz P, Patel A, Lupski JR, Cheung SW.
Nagamani SC, et al. Among authors: chinault c.
Eur J Hum Genet. 2009 May;17(5):573-81. doi: 10.1038/ejhg.2008.220. Epub 2008 Nov 26.
Eur J Hum Genet. 2009.
PMID: 19034313
Free PMC article.
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A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, Seemayer TA, Klein G, Purtilo DT, Sumegi J.
Lanyi A, et al. Among authors: chinault c.
Genomics. 1997 Jan 1;39(1):55-65. doi: 10.1006/geno.1996.4466.
Genomics. 1997.
PMID: 9027486
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