【期刊论文】Bietti Crystalline Corneoretinal Dystrophy Is Caused by Mutations in the Novel Gene CYP4V2
and J. Fielding Hejtmancik, Yuri V. Sergeev, Muriel Kaiser-Kupfer, Xueshan Xiao, Qingjiong Zhang, Elias I. Traboulsi, Richard G. Weleber, John Heckenlively, Richard Alan Lewis, Muh Shy Chen, Atsushi Kanai, Mutsuko Hayakawa, Fumino Iwata, Wenliang Yao,, Daniel F. Schorderet, Francis L. Munier, Xiaodong Jiao,Anren Li,张清炯
【期刊论文】A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612
【期刊论文】A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene
张清炯,Qingjiong Zhang,, Fareeha Zulfiqar, S. Amer Riazuddin, Xueshan Xiao, Afshan Yasmeen, Peter K. Rogan, Raphael Caruso, Paul A. Sieving, Sheikh Riazuddin, J. Fielding Hejtmancik
【期刊论文】Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family
【期刊论文】Mutations in B3-Crystallin Associated with Autosomal Recessive Cataract in Two Pakistani Families
张清炯,S. Amer Riazuddin,, Afshan Yasmeen, Wenliang Yao, Yuri V. Sergeev, Qingjiong Zhang, Fareeha Zulfiqar, Assad Riaz, Sheikh Riazuddin, and J. Fielding Hejtmancik
【期刊论文】Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4
张清炯,Qingjiong Zhang
【期刊论文】A New Locus for Autosomal Recessive Nuclear Cataract Mapped to Chromosome 19q13 in a Pakistani Family
张清炯,S. Amer Riazuddin,, Afshan Yasmeen, Qingjiong Zhang, Wenliang Yao, Muhammad Farooq Sabar, Zahoor Ahmed, Sheikh Riazuddin, and J. Fielding Hejtmancik
【期刊论文】Mutations in the gene encoding the α-subunit of rod phosphodiesterase in consanguineous Pakistani families
张清炯,S. Amer Riazuddin,, Fareeha Zulfiqar, Qingjiong Zhang, Wenliang Yao, Shouling Li, Xiaodong Jiao, Amber Shahzadi, Muhammad Amer, Muhammad Iqbal, Tayyab Hussnain, Paul Sieving, Sheikh
Riazuddin, J. Fielding Hejtmancik
【期刊论文】Linkage analysis of two families with X-linked recessive congenital motor nystagmus
张清炯,Xiangming Guo
【期刊论文】Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation
张清炯,Qingjiong Zhang, Fareeha Zulfiqar, S. Amer Riazuddin,, Xueshan Xiao, Zahoor Ahmad, Sheikh Riazuddin, J. Fielding Hejtmancik
【期刊论文】Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1
张清炯,Xiangming Guo
【期刊论文】Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy
张清炯,Xiaoyun Jia
【期刊论文】Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1
张清炯,Q Zhang, X Guo, X Xiao, X Jia, S Li, J F Hejtmancik
【期刊论文】CSNB1 in Chinese families associated with novel mutations in NYX
张清炯,Xueshan Xiao
【期刊论文】Autosomal Recessive Retinitis Pigmentosa Is Associated with Mutations in RP1 in Three Consanguineous
Pakistani Families
张清炯,S. Amer Riazuddin,, Fareeha Zulfiqar, Qingjiong Zhang, Yuri V. Sergeev, Zaheeruddin A. Qazi, Tayyab Husnain, Rafael Caruso, Sheikh Riazuddin, Paul A. Sieving, and J. Fielding Hejtmancik