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

Author/Creator Zhao, Peiwei

1. 2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotonia. (June 2018)

Authors:: Zhao, Peiwei; Mao, Bing; Cai, Xiaonan; Jiang, Jun; Liu, Zhisheng; Lin, Jun; He, Xuelian
Journal:: International journal of pediatric otorhinolaryngology
Issue:: Volume 109(2018:Jun.)
Page Start:: 96
Record Type:: Journal Article
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2. A 9‐month‐old Chinese patient with Gabriele‐de Vries syndrome due to novel germline mutation in the YY1 gene. Issue 2 (23rd December 2020)

Authors:: Tan, Li; Li, Ying; Liu, Fan; Huang, Yufeng; Luo, Sukun; Zhao, Peiwei; Gu, Weiyue; Lin, Jun; Zhou, Aifen; He, Xuelian
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 9:Issue 2(2021)
Page Start:: n/a
Record Type:: Journal Article
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3. A novel variant in the HX repeat motif of ATN1 in a Chinese patient with CHEDDA syndrome and literature review. Issue 12 (17th October 2022)

Authors:: Luo, Sukun; Hu, Yanqiu; Xiong, Ping; Tan, Li; Zhao, Peiwei; Huang, Yufeng; Xiao, Cuiping; Zhu, Hongmin; He, Xuelian
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 10:Issue 12(2022)
Page Start:: n/a
Record Type:: Journal Article
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4. Genetic analysis and prenatal diagnosis in a Chinese with growth retardation, abnormal liver function, and microcephaly. Issue 9 (31st July 2021)

Authors:: Zhao, Peiwei; Zhang, Lei; Tan, Li; Luo, Sukun; Huang, Yufeng; Peng, Hanming; Cao, Jiangxia; He, Xuelian
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 9:Issue 9(2021)
Page Start:: n/a
Record Type:: Journal Article
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5. Infantile‐onset CMT2D/dSMA‐V in a Chinese family with parental germline mosaicism for a novel mutation in the GARS1 gene. Issue 1 (12th December 2021)

Authors:: Huang, Yufeng; Bi, Bo; Zhao, Peiwei; Yu, Ting; Luo, Sukun; Tan, Li; Liu, Zhisheng; Liu, Jie; He, Xuelian
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 10:Issue 1(2022)
Page Start:: n/a
Record Type:: Journal Article
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6. Influence of UGT2B7 and UGT1A6 polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic children. (3rd July 2021)

Authors:: Du, Zhaosong; Xu, Hua; Zhao, Peiwei; Wang, Jing; Xu, Qiong; Liu, Maochang
Journal:: Xenobiotica
Issue:: Volume 51:Number 7(2021)
Page Start:: 859
Record Type:: Journal Article
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7. Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann–Steiner syndrome. Issue 10 (1st September 2021)

Authors:: Luo, Sukun; Bi, Bo; Zhang, Wenqian; Zhou, Rui; Chen, Wei; Zhao, Peiwei; Huang, Yufeng; Yuan, Li; He, Xuelian
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 9:Issue 10(2021)
Page Start:: n/a
Record Type:: Journal Article
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