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

Year Number of Results
1984 1
1996 1
1997 3
1998 1
1999 1
2001 1
2003 1
2004 1
2011 1
2013 1
2014 1
2015 2
2016 1
2019 2
2020 3
2021 38
2022 222
2023 255
2024 34

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PubMed for id: 355748

500 results

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Page 1
Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Lenassi E, Clayton-Smith J, Douzgou S, Ramsden SC, Ingram S, Hall G, Hardcastle CL, Fletcher TA, Taylor RL, Ellingford JM, Newman WD, Fenerty C, Sharma V, Lloyd IC, Biswas S, Ashworth JL, Black GC, Sergouniotis PI. Lenassi E, et al. Genet Med. 2020 Apr;22(4):745-751. doi: 10.1038/s41436-019-0722-8. Epub 2019 Dec 18. Genet Med. 2020. PMID: 31848469 Free PMC article.
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.
Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.
500 results