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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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2010 | 2 |
2017 | 1 |
2024 | 0 |
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Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Hum Mutat. 2010 Nov;31(11):E1851-60. doi: 10.1002/humu.21362.
Hum Mutat. 2010.
PMID: 20848658
Free PMC article.
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Hamdan FF, Daoud H, Rochefort D, Piton A, Gauthier J, Langlois M, Foomani G, Dobrzeniecka S, Krebs MO, Joober R, Lafrenière RG, Lacaille JC, Mottron L, Drapeau P, Beauchamp MH, Phillips MS, Fombonne E, Rouleau GA, Michaud JL.
Hamdan FF, et al.
Am J Hum Genet. 2010 Nov 12;87(5):671-8. doi: 10.1016/j.ajhg.2010.09.017. Epub 2010 Oct 14.
Am J Hum Genet. 2010.
PMID: 20950788
Free PMC article.
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Prospective investigation of FOXP1 syndrome.
Siper PM, De Rubeis S, Trelles MDP, Durkin A, Di Marino D, Muratet F, Frank Y, Lozano R, Eichler EE, Kelly M, Beighley J, Gerdts J, Wallace AS, Mefford HC, Bernier RA, Kolevzon A, Buxbaum JD.
Siper PM, et al.
Mol Autism. 2017 Oct 24;8:57. doi: 10.1186/s13229-017-0172-6. eCollection 2017.
Mol Autism. 2017.
PMID: 29090079
Free PMC article.
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