• Chinese medical journal · Oct 2018

    Letter Case Reports

    A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn.

    • Hua Zhang, Li-Ming Yang, Lu Yuan, Xin Tan, and Fu-Qing Zhang.
    • Department of Eugenics and Genetics, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China.
    • Chin. Med. J. 2018 Oct 5; 131 (19): 238423852384-2385.

    no abstract available

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