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Year | Number of Results |
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2016 | 1 |
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The parameters to establish a new corneal dystrophy.
Am J Ophthalmol. 2011 Aug;152(2):155-6. doi: 10.1016/j.ajo.2011.04.010.
Am J Ophthalmol. 2011.
PMID: 21784192
Free PMC article.
No abstract available.
Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.
Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG.
Minear MA, et al.
Mol Vis. 2013 Dec 12;19:2508-16. eCollection 2013.
Mol Vis. 2013.
PMID: 24348007
Free PMC article.
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Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.
Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG; FECD Genetics Consortium.
Li YJ, et al.
Invest Ophthalmol Vis Sci. 2014 Jun 10;55(7):4577-84. doi: 10.1167/iovs.13-13517.
Invest Ophthalmol Vis Sci. 2014.
PMID: 24917144
Free PMC article.
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Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections.
Prakash S, Kuang SQ; GenTAC Registry Investigators; Regalado E, Guo D, Milewicz D.
Prakash S, et al.
PLoS One. 2016 Apr 19;11(4):e0153543. doi: 10.1371/journal.pone.0153543. eCollection 2016.
PLoS One. 2016.
PMID: 27092555
Free PMC article.
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Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN, Eghrari AO, Minear MA, Li YJ, Klintworth GK, Afshari N, Gregory SG, Gottsch JD, Katsanis N.
Riazuddin SA, et al.
Am J Hum Genet. 2010 Jan;86(1):45-53. doi: 10.1016/j.ajhg.2009.12.001. Epub 2009 Dec 31.
Am J Hum Genet. 2010.
PMID: 20036349
Free PMC article.
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