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Authors: Li, Lin Nakaya, Naoki Chavali, Venkata R.M. Ma, Zhiwei Hejtmancik, J. Fielding

Citation: Li, Lin et al., A Mutation in ZNF513, a Putative Regulator of Photoreceptor Development, Causes Autosomal-Recessive Retinitis Pigmentosa, American journal of human genetics (Online) AJHG , 87(3), 2010, pp. 400-409

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Citation: Riazuddin, S. Amer et al., A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness, American journal of human genetics (Online) AJHG , 87(4), 2010, pp. 523-531

Authors: Chen, Jianjun Ma, Zhiwei Jiao, Xiaodong Fariss, Robert Hejtmancik, J. Fielding

Citation: Chen, Jianjun et al., Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts, American journal of human genetics (Online) AJHG , 88(6), 2011, pp. 827-838

Authors: Huang, Tim H-M. Hejtmancik, J. Fielding Edwards, Al Pettigrew, Anjana L. Herrera, Carlos A. Hammond, Holly A. Caskey, C. Thomas Zoghbi, Huda Y. Ledbetter, David H.

Citation: Huang, Tim H-m et al., Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26)., American journal of human genetics , 49-II(5), 1991, pp. 1312-1319