Search Results - Chen, Qian-Dui

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  1. 1
    Retinitis pigmentosa with or without skeletal abnormalities due to homozygous mutations in the CWC27 gene: A case report

    Retinitis pigmentosa with or without skeletal abnormalities due to homozygous mutations in the CWC27 gene: A case report by Qi, Yang-Fan, Ma, Xiaoping, Lin, Shuang-Zhu, Wang, Wan-Qi, Li, Jia-Yi, Chen, Qian-Dui, Liu, Li

    Published in Medicine (Baltimore)
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  2. 2
    Eosinophilic granuloma of the clavicle in an 11-year-old Chinese girl: A case report

    Eosinophilic granuloma of the clavicle in an 11-year-old Chinese girl: A case report by Chen, Qian-Dui, Lin, Shuang-Zhu, Zhou, Jie, Chen, Xiao-Xiao, Yang, Rui-Tong, Wang, Xinyao, Li, Jia-Yi, Feng, Xiao-Chun, Liu, Yu-Shu, Jiang, Kai, Feng, Jin-Hua

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  3. 3
    A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report

    A case of West syndrome and global developmental delay in a child with a heterozygous mutation in the TBL1XR1 gene: A case report by Wu, Xiao-Hui, Lin, Shuang-Zhu, Liu, Zhen-Xian, Qi, Yang-Fan, Wang, Wan-Qi, Li, Jia-Yi, Chen, Qian-Dui, Yang, Lu-Lu

    Published in Medicine (Baltimore)
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  4. 4
    Retroperitoneal leiomyoma located in the broad ligament: A case report

    Retroperitoneal leiomyoma located in the broad ligament: A case report by Zhang, Xue-Song, Lin, Shuang-Zhu, Liu, Yu-Jiao, Zhou, Lei, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi

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  5. 5
    Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report

    Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report by Lin, Shuang-Zhu, Ma, Qi-Ji, Pang, Qi-Ming, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi, Zhang, Su-Li

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  6. 6
    VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report

    VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report by Wu, Xiao-Hui, Lin, Shuang-Zhu, Zhou, Yan-Qiu, Wang, Wan-Qi, Li, Jia-Yi, Chen, Qian-Dui

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  7. 7
    Children with infectious pneumonia caused by Ralstonia insidiosa : A case report

    Children with infectious pneumonia caused by Ralstonia insidiosa : A case report by Lin, Shuang-Zhu, Qian, Mei-Jia, Wang, Yan-Wei, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi, Yang, Rui-Tong, Wang, Xin-Yao, Mu, Chun-Yu, Jiang, Kai

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  8. 8
    Retroperitoneal leiomyoma located in the broad ligament: A case report

    Retroperitoneal leiomyoma located in the broad ligament: A case report by Zhang, Xue-Song, Lin, Shuang-Zhu, Liu, Yu-Jiao, Zhou, Lei, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi

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  9. 9
    VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report

    VARS2 gene mutation leading to overall developmental delay in a child with epilepsy: A case report by Wu, Xiao-Hui, Lin, Shuang-Zhu, Zhou, Yan-Qiu, Wang, Wan-Qi, Li, Jia-Yi, Chen, Qian-Dui

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  10. 10
    Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report

    Novel compound heterozygous variants in the LHX3 gene caused combined pituitary hormone deficiency: A case report by Lin, Shuang-Zhu, Ma, Qi-Ji, Pang, Qi-Ming, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi, Zhang, Su-Li

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  11. 11
    Children with infectious pneumonia caused by Ralstonia insidiosa: A case report

    Children with infectious pneumonia caused by Ralstonia insidiosa: A case report by Lin, Shuang-Zhu, Qian, Mei-Jia, Wang, Yan-Wei, Chen, Qian-Dui, Wang, Wan-Qi, Li, Jia-Yi, Yang, Rui-Tong, Wang, Xin-Yao, Mu, Chun-Yu, Jiang, Kai

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