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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1992 1
1993 2
1995 1
1996 2
1997 2
2000 1
2001 3
2003 1
2004 1
2005 2
2006 1
2007 3
2008 1
2010 2
2011 1
2012 1
2013 9
2014 2
2015 3
2016 2
2017 2
2018 1
2019 4
2020 12
2021 3
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59 results
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Page 1
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Autism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, Wright HH, Abramson RK, Betancur C, Bourgeron T, Gillberg C, Leboyer M, Buxbaum JD, Davis KL, Hollander E, Silverman JM, Hallmayer J, Lotspeich L, Sutcliffe JS, Haines JL, Folstein SE, Piven J, Wassink TH, Sheffield V, Geschwind DH, Bucan M, Brown WT, Cantor RM, Constantino JN, Gilliam TC, Herbert M, Lajonchere C, Ledbetter DH, Lese-Martin C, Miller J, Nelson S, Samango-Sprouse CA, Spence S, State M, Tanzi RE, Coon H, Dawson G, Devlin B, Estes A, Flodman P, Klei L, McMahon WM, Minshew N, Munson J, Korvatska E, Rodier PM, Schellenberg GD, Smith M, Spence MA, Stodgell C, Tepper PG, Wijsman EM, Yu CE, Rogé B, Mantoulan C, Wittemeyer K, Poustka A, Felder B, Klauck SM, Schuster C, Poustka F, Bölte S, Feineis-Matthews S, Herbrecht E, Schmötzer G, Tsiantis J, Papanikolaou K, Maestrini E, Bacchelli E, Blasi F, Carone S, Toma C, Van Engeland H, de Jonge M, Kemner C, Koop F, Langemeijer M, Hijmans C, Staal WG, Baird G, Bolton PF, Rutter ML, Weisblatt E, Green J, Aldred C, Wilkinson JA, Pickles A, Le Couteur A, Berney T, McConachie H, Bailey AJ, Francis K, Honeyman G, Hutchinson A, Parr JR, Wallace S, Monaco AP, Barnby G, Kobayashi K, Lamb JA, Sousa I, Sykes N, Cook EH, Guter SJ, Leventhal BL, Salt J, Lord C, Corsello C, Hus V, Weeks DE, Volkmar F, Tauber M, Fombonne E, Shih A, Meyer KJ. Autism Genome Project Consortium, et al. Among authors: samango sprouse ca. Nat Genet. 2007 Mar;39(3):319-28. doi: 10.1038/ng1985. Epub 2007 Feb 18. Nat Genet. 2007. PMID: 17322880 Free PMC article.
Neurocognitive development and capabilities in boys with 49,XXXXY syndrome.
Gropman AL, Porter GF, Lasutschinkow PC, Sadeghin T, Tipton ES, Powell S, Samango-Sprouse CA. Gropman AL, et al. Among authors: samango sprouse ca. Am J Med Genet A. 2020 Jul 14. doi: 10.1002/ajmg.a.61736. Online ahead of print. Am J Med Genet A. 2020. PMID: 32662248
Speech and language development in children with 49,XXXXY syndrome.
Samango-Sprouse CA, Lasutschinkow PC, McLeod M, Porter GF, Powell S, St Laurent J, Sadeghin T, Gropman AL. Samango-Sprouse CA, et al. Am J Med Genet A. 2020 Jul 28. doi: 10.1002/ajmg.a.61767. Online ahead of print. Am J Med Genet A. 2020. PMID: 32725750
Prenatal diagnosis and 47,XXY.
Simpson JL, Samango-Sprouse C. Simpson JL, et al. Among authors: samango sprouse c. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):64-70. doi: 10.1002/ajmg.c.31356. Am J Med Genet C Semin Med Genet. 2013. PMID: 23359597 Review.
Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY.
Tosi L, Mitchell F, Porter GF, Ruland L, Gropman A, Lasutschinkow PC, Tran SL, Rajah EN, Gillies AP, Hendrie P, Peret R, Sadeghin T, Samango-Sprouse CA. Tosi L, et al. Among authors: samango sprouse ca. Am J Med Genet A. 2020 Apr 3. doi: 10.1002/ajmg.a.61578. Online ahead of print. Am J Med Genet A. 2020. PMID: 32243688
59 results
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