Author/Creator: Xing, Xiao‐ping - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Xing, Xiao‐ping

1. A novel mutation in PLS3 causes extremely rare X‐linked osteogenesis imperfecta. Issue 12 (9th November 2020)

Authors:: Hu, Jing; Li, Lu‐jiao; Zheng, Wen‐bin; Zhao, Di‐chen; Wang, Ou; Jiang, Yan; Xing, Xiao‐ping; Li, Mei; Xia, Weibo
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 8:Issue 12(2020)
Page Start:: n/a
Record Type:: Journal Article
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2. Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita. Issue 3 (23rd January 2020)

Authors:: Zheng, Wen‐bin; Li, Lu‐jiao; Zhao, Di‐chen; Wang, Ou; Jiang, Yan; Xia, Wei‐bo; Xing, Xiao‐ping; Li, Mei
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 8:Issue 3(2020)
Page Start:: n/a
Record Type:: Journal Article
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