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

Year Number of Results
1993 1
2009 1
2018 1
2019 1
2020 2
2021 2
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5 results
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Page 1
Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant.
Thomas MG, Maconachie GDE, Constantinescu CS, Chan WM, Barry B, Hisaund M, Sheth V, Kuht HJ, Dineen RA, Harieaswar S, Engle EC, Gottlob I. Thomas MG, et al. Among authors: hisaund m. Br J Ophthalmol. 2020 Apr;104(4):547-550. doi: 10.1136/bjophthalmol-2019-314293. Epub 2019 Jul 13. Br J Ophthalmol. 2020. PMID: 31302631 Free PMC article.
FRMD7-Related Infantile Nystagmus.
Thomas MG, Maconachie G, Hisaund M, Gottlob I. Thomas MG, et al. Among authors: hisaund m. 2009 Feb 12 [updated 2018 Aug 16]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. 2009 Feb 12 [updated 2018 Aug 16]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. PMID: 20301748 Free Books & Documents. Review.
Discordant phenotypes in twins with infantile nystagmus.
Aamir A, Kuht HJ, McLean RJ, Maconachie GDE, Sheth V, Dawar B, Purohit R, Sylvius N, Hisaund M, Zubcov-Iwantscheff A, Proudlock FA, Gottlob I, Thomas MG. Aamir A, et al. Among authors: hisaund m. Sci Rep. 2021 Feb 2;11(1):2826. doi: 10.1038/s41598-021-82368-0. Sci Rep. 2021. PMID: 33531592 Free PMC article.