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RESEARCH REPORT

Hereditary High Hypermetropia in the Faroe Islands

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Pages 9-15 | Accepted 02 Aug 2004, Published online: 08 Jul 2009

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Justin C. Sherwin, Alex W. Hewitt, Jonathan B. Ruddle & David A. Mackey. (2008) Genetic Isolates in Ophthalmic Diseases. Ophthalmic Genetics 29:4, pages 149-161.
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Shijin Wen, Xiaoshan Min, Ying Zhu & Xia Zhou. (2022) Genetic analysis assists diagnosis of clinical systemic disease in children with excessive hyperopia. BMC Pediatrics 22:1.
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Xueshan Xiao, Wenmin Sun, Jiamin Ouyang, Shiqiang Li, Xiaoyun Jia, Zhiqun Tan, J. Fielding Hejtmancik & Qingjiong Zhang. (2019) Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3. Human Genetics 138:10, pages 1077-1090.
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Nikisha Q. Richards, Adam Pflugrath, Chetna Pande & Natario L. Couser. 2019. Ophthalmic Genetic Diseases. Ophthalmic Genetic Diseases 41 52 .
Yan Xu, Liping Guan, Xueshan Xiao, Jianguo Zhang, Shiqiang Li, Hui Jiang, Xiaoyun Jia, Ye Yin, Xiangming Guo, Zhikuan Yang & Qingjiong Zhang. (2016) Identification of MFRP Mutations in Chinese Families with High Hyperopia. Optometry and Vision Science 93:1, pages 19-26.
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Myron Yanoff & Joseph W. Sassani. 2015. Ocular Pathology. Ocular Pathology 555 588.e7 .
Hans C. Fledelius, Ernst Goldschmidt, Birgitte Haargaard & Hanne Jensen. (2014) Human parallels to experimental myopia? A literature review on visual deprivation. Acta Ophthalmologica 92:8, pages 724-729.
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Sawsan R. Nowilaty, Arif O. Khan, Mohammed A. Aldahmesh, Khalid F. Tabbara, Abdullah Al-Amri & Fowzan S. Alkuraya. (2013) Biometric and Molecular Characterization of Clinically Diagnosed Posterior Microphthalmos. American Journal of Ophthalmology 155:2, pages 361-372.e7.
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Itsuka Matsushita, Hiroyuki Kondo & Akihiko Tawara. (2012) Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmos. Japanese Journal of Ophthalmology 56:4, pages 396-400.
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Andreas Gal, Isabella Rau, Leila El Matri, Hans-Jürgen Kreienkamp, Susanne Fehr, Karim Baklouti, Ibtissem Chouchane, Yun Li, Monika Rehbein, Josefine Fuchs, Hans C. Fledelius, Kaj Vilhelmsen, Daniel F. Schorderet, Francis L. Munier, Elsebet Ostergaard, Debra A. Thompson & Thomas Rosenberg. (2011) Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease. The American Journal of Human Genetics 88:3, pages 382-390.
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Sandrine Paget, Zulma G. Vitezica, François Malecaze & Patrick Calvas. (2008) Heritability of refractive value and ocular biometrics. Experimental Eye Research 86:2, pages 290-295.
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Tien Tay, James EH Smith, Yemima Berman, Lesley Adès, Isabelle Missotte, Hēlène Saglibène, Frank Martin, Paul Mitchell & David Taylor. (2007) Nanophthalmos in a Melanesian population. Clinical & Experimental Ophthalmology 35:4, pages 348-354.
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KRISTINA TARCZY-HORNOCH. (2007) The Epidemiology of Early Childhood Hyperopia. Optometry and Vision Science 84:2, pages 115-123.
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