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

Year Number of Results
1995 1
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1998 1
2000 2
2001 5
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2024 0

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PubMed (OMIM) for id: 390767

13 results

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Page 1
Presence of large deletions in kindreds with autism.
Yu CE, Dawson G, Munson J, D'Souza I, Osterling J, Estes A, Leutenegger AL, Flodman P, Smith M, Raskind WH, Spence MA, McMahon W, Wijsman EM, Schellenberg GD. Yu CE, et al. Am J Hum Genet. 2002 Jul;71(1):100-15. doi: 10.1086/341291. Epub 2002 Jun 7. Am J Hum Genet. 2002. PMID: 12058345 Free PMC article.
Evidence supporting WNT2 as an autism susceptibility gene.
Wassink TH, Piven J, Vieland VJ, Huang J, Swiderski RE, Pietila J, Braun T, Beck G, Folstein SE, Haines JL, Sheffield VC. Wassink TH, et al. Am J Med Genet. 2001 Jul 8;105(5):406-13. doi: 10.1002/ajmg.1401. Am J Med Genet. 2001. PMID: 11449391
Chromosome 7q: where autism meets language disorder?
Folstein SE, Mankoski RE. Folstein SE, et al. Am J Hum Genet. 2000 Aug;67(2):278-81. doi: 10.1086/303034. Epub 2000 Jul 7. Am J Hum Genet. 2000. PMID: 10889044 Free PMC article. No abstract available.
13 results