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Year Number of Results
2011 2
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2013 2
2014 2
2015 1
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2020 6
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2023 5
2024 0

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Page 1
Xp11.3 microdeletion causing Norrie disease and X-linked Kabuki syndrome.
Mansoor M, Coussa RG, Strampe MR, Larson SA, Russell JF. Mansoor M, et al. Among authors: coussa rg. Am J Ophthalmol Case Rep. 2023 Jan 19;29:101798. doi: 10.1016/j.ajoc.2023.101798. eCollection 2023 Mar. Am J Ophthalmol Case Rep. 2023. PMID: 36703904 Free PMC article.
Genetic Diagnosis for 64 Patients with Inherited Retinal Disease.
Lynn J, Raney A, Britton N, Ramoin J, Yang RW, Radojevic B, McClard CK, Kingsley R, Coussa RG, Bennett LD. Lynn J, et al. Among authors: coussa rg. Genes (Basel). 2022 Dec 26;14(1):74. doi: 10.3390/genes14010074. Genes (Basel). 2022. PMID: 36672815 Free PMC article.
40 results