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

Year Number of Results
2011 1
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2017 5
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2020 5
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2024 2
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37 results

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Page 1
The evolving role of genetics in ophthalmology.
Couser NL, Brooks BP, Drack AV, Shankar SP. Couser NL, et al. Ophthalmic Genet. 2021 Apr;42(2):110-113. doi: 10.1080/13816810.2020.1868011. Epub 2021 Jan 12. Ophthalmic Genet. 2021. PMID: 33432855 Free PMC article. Review.
Camptodactyly and the 22q11.2 deletion syndrome.
Couser NL, Pande CK, Walsh JM, Tepperberg J, Aylsworth AS. Couser NL, et al. Am J Med Genet A. 2017 Feb;173(2):515-518. doi: 10.1002/ajmg.a.38029. Epub 2016 Oct 28. Am J Med Genet A. 2017. PMID: 27792854
Ocular Manifestations of the NAA10-Related Syndrome.
Gupta AS, Saif HA, Lent JM, Couser NL. Gupta AS, et al. Among authors: couser nl. Case Rep Genet. 2019 Apr 8;2019:8492965. doi: 10.1155/2019/8492965. eCollection 2019. Case Rep Genet. 2019. PMID: 31093388 Free PMC article.
Eye manifestations in the NSUN2 intellectual disability syndrome.
Pingree G, Harper A, Snajczuk J, Couser NL. Pingree G, et al. Among authors: couser nl. Int J Mol Epidemiol Genet. 2021 Dec 15;12(6):129-134. eCollection 2021. Int J Mol Epidemiol Genet. 2021. PMID: 35126837 Free PMC article.
Ocular manifestations of Nabais Sa-de Vries Syndrome type 1.
Zhang L, King K, Couser NL. Zhang L, et al. Among authors: couser nl. Int J Mol Epidemiol Genet. 2022 Jun 15;13(1):15-23. eCollection 2022. Int J Mol Epidemiol Genet. 2022. PMID: 35892095 Free PMC article.
37 results