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The complete genome of an individual by massively parallel DNA sequencing.
Nature. 2008 Apr 17;452(7189):872-6. doi: 10.1038/nature06884.
Nature. 2008.
PMID: 18421352
The DNA sequence of the human X chromosome.
Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, Sudbrak R, Wen G, Jones MC, Hurles ME, Andrews TD, Scott CE, Searle S, Ramser J, Whittaker A, Deadman R, Carter NP, Hunt SE, Chen R, Cree A, Gunaratne P, Havlak P, Hodgson A, Metzker ML, Richards S, Scott G, Steffen D, Sodergren E, Wheeler DA, Worley KC, Ainscough R, Ambrose KD, Ansari-Lari MA, Aradhya S, Ashwell RI, Babbage AK, Bagguley CL, Ballabio A, Banerjee R, Barker GE, Barlow KF, Barrett IP, Bates KN, Beare DM, Beasley H, Beasley O, Beck A, Bethel G, Blechschmidt K, Brady N, Bray-Allen S, Bridgeman AM, Brown AJ, Brown MJ, Bonnin D, Bruford EA, Buhay C, Burch P, Burford D, Burgess J, Burrill W, Burton J, Bye JM, Carder C, Carrel L, Chako J, Chapman JC, Chavez D, Chen E, Chen G, Chen Y, Chen Z, Chinault C, Ciccodicola A, Clark SY, Clarke G, Clee CM, Clegg S, Clerc-Blankenburg K, Clifford K, Cobley V, Cole CG, Conquer JS, Corby N, Connor RE, David R, Davies J, Davis C, Davis J, Delgado O, Deshazo D, Dhami P, Ding Y, Dinh H, Dodsworth S, Draper H, Dugan-Rocha S, Dunham A, Dunn M, Durbin KJ, Dutta I, Eades T, Ellwood…
See abstract for full author list ➔
Ross MT, et al. Among authors: chinault c.
Nature. 2005 Mar 17;434(7031):325-37. doi: 10.1038/nature03440.
Nature. 2005.
PMID: 15772651
Free PMC article.
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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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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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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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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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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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