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Ophthalmic Genetics Volume 34, 2013 - Issue 3
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Letter

Novel Homozygous CYP1B1 Deletion in Siblings with Primary Congenital Glaucoma

Kristy DamjanovichARUP Institute for Clinical and Experimental Pathology Salt Lake City, UTUSA
,
Erin E. BaldwinARUP Institute for Clinical and Experimental Pathology Salt Lake City, UTUSA
,
Tracey LewisARUP Institute for Clinical and Experimental Pathology Salt Lake City, UTUSA
&
Pinar Bayrak-ToydemirARUP Institute for Clinical and Experimental Pathology Salt Lake City, UTUSA;Department of Pathology, University of Utah Salt Lake City, UTUSACorrespondence[email protected]
Pages 180-181 | Received 26 Jun 2012, Accepted 15 Oct 2012, Published online: 06 Dec 2012

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Murad Khan, Suleman Shah, Baixue Lv, Zhanjun Lv, Ning Ji, Zhixue Song, Peiyuan Wu, Xiufang Wang & Arshad Mehmood. (2023) Molecular Mechanisms of Alu and LINE-1 Interspersed Repetitive Sequences Reveal Diseases of Visual System Dysfunction. Ocular Immunology and Inflammation 31:9, pages 1848-1858.
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Articles from other publishers (2)

Emmanuelle Souzeau, Andrew Dubowsky, Jonathan B. Ruddle & Jamie E. Craig. (2019) Primary congenital glaucoma due to paternal uniparental isodisomy of chromosome 2 and CYP1B1 deletion . Molecular Genetics & Genomic Medicine 7:8.
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Adam P. DeLuca, Wallace L.M. Alward, Jeffrey Liebmann, Robert Ritch, Kazuhide Kawase, Young H. Kwon, Alan L. Robin, Edwin M. Stone, Todd E. Scheetz & John H. Fingert. (2017) Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients. Journal of Glaucoma 26:12, pages 1063-1067.
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