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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 1 |
2008 | 1 |
2009 | 1 |
2024 | 0 |
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A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Ann Hum Genet. 2009 May;73(Pt 3):263-73. doi: 10.1111/j.1469-1809.2009.00523.x.
Ann Hum Genet. 2009.
PMID: 19456320
Free PMC article.
Examination of association to autism of common genetic variationin genes related to dopamine.
Anderson BM, Schnetz-Boutaud N, Bartlett J, Wright HH, Abramson RK, Cuccaro ML, Gilbert JR, Pericak-Vance MA, Haines JL.
Anderson BM, et al.
Autism Res. 2008 Dec;1(6):364-9. doi: 10.1002/aur.55.
Autism Res. 2008.
PMID: 19360691
Free PMC article.
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High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35.
Stamm DS, Rampersaud E, Slifer SH, Mehltretter L, Siegel DG, Xie J, Hu-Lince D, Craig DW, Stephan DA, George TM, Gilbert JR, Speer MC; NTD Collaborative Group.
Stamm DS, et al.
Birth Defects Res A Clin Mol Teratol. 2006 Jun;76(6):499-505. doi: 10.1002/bdra.20272.
Birth Defects Res A Clin Mol Teratol. 2006.
PMID: 16933213
Free PMC article.
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