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Axenfeld Rieger syndrome journal articles from PubMed MEDLINE database

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Reis LM, Tyler RC, Volkmann Kloss BA, et al. 
PITX2 and FOXC1 spectrum of mutations in ocular syndromes. [JOURNAL ARTICLE]
Eur J Hum Genet 2012 May 9.
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Mao M, Solivan-Timpe F, Roos BR, et al. 
Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma. [Journal Article]
Mol Vis 2012.:705-13.
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Sauer A, Speeg-Schatz C 
[Axenfeld-Rieger syndrome]. [Journal Article]
J Fr Ophtalmol 2012 May; 35(5):392.
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François M, Ramchandran R 
Studies on Axenfeld-Rieger syndrome patients and mice reveal Foxc1's role in corneal neovascularization. [Comment, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Proc Natl Acad Sci U S A 2012 Feb 7; 109(6):1818-9.
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Liu Y, Semina EV 
pitx2 deficiency results in abnormal ocular and craniofacial development in zebrafish. [Journal Article, Research Support, N.I.H., Extramural]
PLoS One 2012; 7(1):e30896.
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Chang TC, Summers CG, Schimmenti LA, et al. 
Axenfeld-Rieger syndrome: new perspectives. [Journal Article, Review]
Br J Ophthalmol 2012 Mar; 96(3):318-22.
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Seo S, Singh HP, Lacal PM, et al. 
Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Proc Natl Acad Sci U S A 2012 Feb 7; 109(6):2015-20.
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Bohnsack BL, Kasprick DS, Kish PE, et al. 
A zebrafish model of axenfeld-rieger syndrome reveals that pitx2 regulation by retinoic acid is essential for ocular and craniofacial development. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Invest Ophthalmol Vis Sci 2012 Jan; 53(1):7-22.
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Berenstein-Aizman G, Hazan-Molina H, Drori D, et al. 
Axenfeld-Rieger syndrome: dentofacial manifestation and oral rehabilitation considerations. [Journal Article]
Pediatr Dent 2011 Sep-Oct; 33(5):440-4.
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Tonoki H, Harada N, Shimokawa O, et al. 
Axenfeld-Rieger anomaly and Axenfeld-Rieger syndrome: clinical, molecular-cytogenetic, and DNA array analyses of three patients with chromosomal defects at 6p25. [Case Reports, Journal Article]
Am J Med Genet A 2011 Dec; 155A(12):2925-32.
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