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Identification of compound heterozygous deletion of the WWOX gene in WOREE syndrome by Xing-sheng Dong, Xiao-jun Wen, Sheng Zhang, De-gang Wang, Yi Xiong, Zhi-ming Li
Published 2023-11-01
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A familial Cri-du-Chat/5p deletion syndrome resulted from rare maternal complex chromosomal rearrangements (CCRs) and/or possible chromosome 5p chromothripsis. by Heng Gu, Jian-hui Jiang, Jian-ying Li, Ya-nan Zhang, Xing-sheng Dong, Yang-yu Huang, Xin-ming Son, Xinyan Lu, Zheng Chen
Published 2013-01-01
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