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Page 1
Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy.
Hum Mutat. 2007 Jun;28(6):638. doi: 10.1002/humu.9495.
Hum Mutat. 2007.
PMID: 17437275
Free PMC article.
British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene.
Liskova P, Prescott Q, Bhattacharya SS, Tuft SJ.
Liskova P, et al. Among authors: prescott q.
Br J Ophthalmol. 2007 Dec;91(12):1717-8. doi: 10.1136/bjo.2007.115154.
Br J Ophthalmol. 2007.
PMID: 18024822
Free PMC article.
No abstract available.
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A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract.
Berry V, Francis PJ, Prescott Q, Waseem NH, Moore AT, Bhattacharya SS.
Berry V, et al. Among authors: prescott q.
Mol Vis. 2011;17:1249-53. Epub 2011 May 6.
Mol Vis. 2011.
PMID: 21633712
Free PMC article.
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Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing.
Aung T, Ebenezer ND, Brice G, Child AH, Prescott Q, Lehmann OJ, Hitchings RA, Bhattacharya SS.
Aung T, et al. Among authors: prescott q.
J Med Genet. 2003 Aug;40(8):e101. doi: 10.1136/jmg.40.8.e101.
J Med Genet. 2003.
PMID: 12920093
Free PMC article.
No abstract available.
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Dominant cataract formation in association with a vimentin assembly disrupting mutation.
Müller M, Bhattacharya SS, Moore T, Prescott Q, Wedig T, Herrmann H, Magin TM.
Müller M, et al. Among authors: prescott q.
Hum Mol Genet. 2009 Mar 15;18(6):1052-7. doi: 10.1093/hmg/ddn440. Epub 2009 Jan 6.
Hum Mol Genet. 2009.
PMID: 19126778
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Characterisation of phosphoglycerate kinase genes in Leishmania major and evidence for the absence of a third closely related gene or isoenzyme.
McKoy G, Badal M, Prescott Q, Lux H, Hart DT.
McKoy G, et al. Among authors: prescott q.
Mol Biochem Parasitol. 1997 Dec 1;90(1):169-81. doi: 10.1016/s0166-6851(97)00172-2.
Mol Biochem Parasitol. 1997.
PMID: 9497041
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