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

Year Number of Results
1974 1
2000 1
2003 1
2013 1
2014 1
2015 2
2018 1
2019 2
2020 1
2022 2
2024 0

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11 results

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Page 1
A novel noncoding FKRP mutation in early onset limb-girdle muscular dystrophy.
Saylam E, Moore SA, Aravindhan A, Marton H, Nagy PL, Gokden M, Cox MO, Stefans V, Veerapandiyan A. Saylam E, et al. Among authors: cox mo. Neurol Genet. 2019 Dec 26;6(1):e388. doi: 10.1212/NXG.0000000000000388. eCollection 2020 Feb. Neurol Genet. 2019. PMID: 32042916 Free PMC article. No abstract available.
Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>G.
Lee AJ, Jones KA, Butterfield RJ, Cox MO, Konersman CG, Grosmann C, Abdenur JE, Boyer M, Beson B, Wang C, Dowling JJ, Gibbons MA, Ballard A, Janas JS, Leshner RT, Donkervoort S, Bönnemann CG, Malicki DM, Weiss RB, Moore SA, Mathews KD. Lee AJ, et al. Among authors: cox mo. Neurol Genet. 2019 Mar 1;5(2):e315. doi: 10.1212/NXG.0000000000000315. eCollection 2019 Apr. Neurol Genet. 2019. PMID: 31041397 Free PMC article.
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.
Davidson AE, Siddiqui FM, Lopez MA, Lunt P, Carlson HA, Moore BE, Love S, Born DE, Roper H, Majumdar A, Jayadev S, Underhill HR, Smith CO, von der Hagen M, Hubner A, Jardine P, Merrison A, Curtis E, Cullup T, Jungbluth H, Cox MO, Winder TL, Abdel Salam H, Li JZ, Moore SA, Dowling JJ. Davidson AE, et al. Among authors: cox mo. Brain. 2013 Feb;136(Pt 2):508-21. doi: 10.1093/brain/aws344. Brain. 2013. PMID: 23413262 Free PMC article.
Oral leukocytes and gingivitis in the primary dentition.
Cox MO, Crawford JJ, Lundblad RL, McFall WT Jr. Cox MO, et al. J Periodontal Res. 1974;9(1):23-8. doi: 10.1111/j.1600-0765.1974.tb00649.x. J Periodontal Res. 1974. PMID: 4152984 No abstract available.
11 results