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Ophthalmic Genetics Volume 16, 1995 - Issue 3
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Original Article

X-linked retinitis pigmentosa: re-evaluation of fundus findings and the use of haplotype analysis in clarification of carrier female status

N. T. Bech-Hansen Molecular Genetics Unit, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada
&
W. G. Pearce Department of Ophthalmology, University of Alberta, Edmonton, Alberta, Canada
Pages 113-118 | Accepted 20 Jun 1995, Published online: 08 Jul 2009

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Saradha Iragavarapu & Michael B. Gorin. (2015) Gender Specific Issues in Hereditary Ocular Disorders. Current Eye Research 40:2, pages 128-145.
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Articles from other publishers (2)

An-Lun WuJung-Pan WangYun-Ju Tseng, Laura LiuYu-Chuan KangKuan-Jen ChenAn-Ning ChaoLung-Kun YehTun-Lu ChenYih-Shiou HwangWei-Chi WuChi-Chun LaiNan-Kai Wang. (2018) MULTIMODAL IMAGING OF MOSAIC RETINOPATHY IN CARRIERS OF HEREDITARY X-LINKED RECESSIVE DISEASES. Retina 38:5, pages 1047-1057.
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Sung Pyo Park, In Hwan Hong, Stephen H Tsang & Stanley Chang. (2013) Cellular imaging demonstrates genetic mosaicism in heterozygous carriers of an X-linked ciliopathy gene. European Journal of Human Genetics 21:11, pages 1240-1248.
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