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

Year Number of Results
1973 1
1979 1
1980 2
1981 1
1983 1
1984 2
1985 3
1986 1
1988 1
1989 4
1990 1
1991 3
1992 2
1993 4
1994 3
1995 8
1996 5
1998 1
1999 2
2000 4
2001 1
2002 2
2003 3
2005 1
2006 1
2008 2
2009 1
2011 1
2012 3
2013 1
2014 1
2015 1
2016 6
2017 5
2018 5
2021 0
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80 results
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Page 1
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF, Bartell T, Bernstein JA, Beyer E, Blumenthal I, Bongers EM, Brilstra EH, Brown CW, Br├╝ggenwirth HT, Callewaert B, Chiang C, Corning K, Cox H, Cuppen E, Currall BB, Cushing T, David D, Deardorff MA, Dheedene A, D'Hooghe M, de Vries BB, Earl DL, Ferguson HL, Fisher H, FitzPatrick DR, Gerrol P, Giachino D, Glessner JT, Gliem T, Grady M, Graham BH, Griffis C, Gripp KW, Gropman AL, Hanson-Kahn A, Harris DJ, Hayden MA, Hill R, Hochstenbach R, Hoffman JD, Hopkin RJ, Hubshman MW, Innes AM, Irons M, Irving M, Jacobsen JC, Janssens S, Jewett T, Johnson JP, Jongmans MC, Kahler SG, Koolen DA, Korzelius J, Kroisel PM, Lacassie Y, Lawless W, Lemyre E, Leppig K, Levin AV, Li H, Li H, Liao EC, Lim C, Lose EJ, Lucente D, Macera MJ, Manavalan P, Mandrile G, Marcelis CL, Margolin L, Mason T, Masser-Frye D, McClellan MW, Mendoza CJ, Menten B, Middelkamp S, Mikami LR, Moe E, Mohammed S, Mononen T, Mortenson ME, Moya G, Nieuwint AW, Ordulu Z, Parkash S, Pauker SP, Pereira S, Perrin D, Phelan K, Aguilar RE, Poddighe PJ, Pregno G, Raskin S, Reis L, Rhead W, Rita D, Renkens I, Roelens F, Ruliera J, Rump P, Schilit SL, Shaheen R, Sparkes R, Spiegel E, Stevens B, Stone MR, Tagoe J, Thakuria JV, van Bon BW, van de Kamp J, van Der Burgt I, van Essen T, van Ravenswaaij-Arts CM, van Roosmalen MJ, Vergult S, Volker-Touw CM, Warburton DP, Waterman MJ, Wiley S, Wilson A, Yerena-de Vega MC, Zori RT, Levy B, Brunner HG, de Leeuw N, Kloosterman WP, Thorland EC, Morton CC, Gusella JF, Talkowski ME. Redin C, et al. Among authors: kahler sg. Nat Genet. 2017 Jan;49(1):36-45. doi: 10.1038/ng.3720. Epub 2016 Nov 14. Nat Genet. 2017. PMID: 27841880 Free PMC article.
Autism and environmental genomics.
Herbert MR, Russo JP, Yang S, Roohi J, Blaxill M, Kahler SG, Cremer L, Hatchwell E. Herbert MR, et al. Among authors: kahler sg. Neurotoxicology. 2006 Sep;27(5):671-84. doi: 10.1016/j.neuro.2006.03.017. Epub 2006 Mar 28. Neurotoxicology. 2006. PMID: 16644012 Review.
Metabolic disorders and mental retardation.
Kahler SG, Fahey MC. Kahler SG, et al. Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):31-41. doi: 10.1002/ajmg.c.10018. Am J Med Genet C Semin Med Genet. 2003. PMID: 12561056 Review.
Carnitine homeostasis in the organic acidurias.
Roe CR, Millington DS, Kahler SG, Kodo N, Norwood DL. Roe CR, et al. Among authors: kahler sg. Prog Clin Biol Res. 1990;321:383-402. Prog Clin Biol Res. 1990. PMID: 2183238 Review.
Fryns syndrome survivors and neurologic outcome.
Van Hove JL, Spiridigliozzi GA, Heinz R, McConkie-Rosell A, Iafolla AK, Kahler SG. Van Hove JL, et al. Among authors: kahler sg. Am J Med Genet. 1995 Nov 20;59(3):334-40. doi: 10.1002/ajmg.1320590311. Am J Med Genet. 1995. PMID: 8599357 Review.
Galactosaemia in Chinese.
Kahler SG. Kahler SG. J Paediatr Child Health. 1999 Aug;35(4):339-440. J Paediatr Child Health. 1999. PMID: 10457287 No abstract available.
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