Author/Creator: Zheng, Shushen - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Zheng, Shushen

1. A novel EDA1 missense mutation in X-linked hypohidrotic ectodermal dysplasia. Issue 11 (March 2020)

Authors:: Wang, Xu; Zhang, Zhiyu; Yuan, Shuo; Ren, Jiabao; Qu, Hong; Zhang, Guozhong; Chen, Wenjing; Zheng, Shushen; Meng, Lingqiang; Bai, Jiuping; Du, Qingqing; Yang, Dongru; Shen, Wenjing
Other Names:: Jain. Nikhil section editor.
Journal:: Medicine
Issue:: Volume 99:Issue 11(2020)
Page Start:
Record Type:: Journal Article
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2. Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasia. Issue 45 (12th November 2021)

Authors:: Yang, Liyuan; Lu, Genqi; Shen, Wenjing; Chen, Wenjing; Lu, Haiyan; Zhang, Guozhong; Yuan, Shuo; Zheng, Shushen; Ren, Jiabao
Other Names:: Ali. Shereen section editor.
Journal:: Medicine
Issue:: Volume 100:Issue 45(2021)
Page Start:
Record Type:: Journal Article
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3. Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasia. Issue 45 (12th November 2021)

Authors:: Yang, Liyuan; Lu, Genqi; Shen, Wenjing; Chen, Wenjing; Lu, Haiyan; Zhang, Guozhong; Yuan, Shuo; Zheng, Shushen; Ren, Jiabao
Editors:: Ali., Shereen
Journal:: Medicine
Issue:: Volume 100:Issue 45(2021)
Page Start:: e27746
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗