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Items: 4

1.
Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular muscles
Gang Liu, Xue Chen, Xiantao Sun, Hu Liu, Kanxing Zhao, Qinglin Chang, Xinyuan Pan, Xiuying Wang, Songtao Yuan, Qinghuai Liu, Chen Zhao
Mol Vis. 2014; 20: 15–23. Published online 2014 Jan 6.
PMCID:
PMC3888497
AbstractArticlePDF–2.6M
2.
Evidence of an Asymmetrical Endophenotype in Congenital Fibrosis of Extraocular Muscles Type 3 Resulting from TUBB3 Mutations
Joseph L. Demer, Robert A. Clark, Max A. Tischfield, Elizabeth C. Engle
Invest Ophthalmol Vis Sci. 2010 Sep; 51(9): 4600–4611. doi: 10.1167/iovs.10-5438
PMCID:
PMC2941178
AbstractArticlePDF–3.0M
3.
Anomalous Scleral Insertion of Superior Oblique in Axenfeld-Rieger Syndrome
Sang Woo Park, Hwang Gyun Kim, Hwan Heo, Yeoung Geol Park
Korean J Ophthalmol. 2009 Mar; 23(1): 62–64. Published online 2009 Mar 9. doi: 10.3341/kjo.2009.23.1.62
PMCID:
PMC2655743
AbstractArticlePDF–1.8M
4.
Magnetic Resonance Imaging Evidence for Widespread Orbital Dysinnervation in Dominant Duane’s Retraction Syndrome Linked to the DURS2 Locus
Joseph L. Demer, Robert A. Clark, Key-Hwan Lim, Elizabeth C. Engle
Invest Ophthalmol Vis Sci. Author manuscript; available in PMC 2008 Jan 1.
Published in final edited form as: Invest Ophthalmol Vis Sci. 2007 Jan; 48(1): 194–202. doi: 10.1167/iovs.06-0632
PMCID:
PMC1850629
AbstractArticlePDF–958K

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