De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia by Xiaoyu Huang, Xue Rui, Shuang Zhang, Xiaolong Qi, Weining Rong, Xunlun Sheng

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Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families by Feiyin Zi, Zhen Li, Wanyu Cheng, Xiaoyu Huang, Xunlun Sheng, Weining Rong

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Four different gene-related cone–rod dystrophy: clinical and genetic findings in six Chinese families with diverse modes of inheritance by Zhen Li, Wanyu Cheng, Feiyin Zi, Juan Wang, Xiaoyu Huang, Xunlun Sheng, Weining Rong

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BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity by Shangying Yang, Zhen Li, Wanyu Cheng, Meijiao Ma, Rui Qi, Xue Rui, Yinghua Ren, Xunlun Sheng, Weining Rong

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Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2. by Weining Rong, Xue Chen, Kanxing Zhao, Yani Liu, Xiaoxing Liu, Shaoping Ha, Wenzhou Liu, Xiaoli Kang, Xunlun Sheng, Chen Zhao

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Two novel variations in LRP2 cause Donnai-Barrow syndrome in a Chinese family with severe early-onset high myopia by Shiqin Yuan, Xiaoyu Huang, Xiaoyu Huang, Shuang Zhang, Shangying Yang, Shangying Yang, Xue Rui, Xiaolong Qi, Xuhui Wang, Yali Zheng, Weining Rong, Xunlun Sheng

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