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Microbiology (Reading, England)
|
August 22, 2009
Identification and characterization of a novel spore-associated subtilase from Thermoactinomyces sp. CDF
Guyue Cheng, Peiwei Zhao, Xiao-Feng Tang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 10, 2018
[Clinical features and genetic analysis of a case with Coffin-Siris syndrome]
Peiwei Zhao, Dan Gao, Yufeng Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
February 1, 2019
[Genome-wide copy number microarray analysis for a boy with autism]
Xuelian He, Peiwei Zhao, Yufeng Huang, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
May 18, 2021
Influence of <i>UGT2B7</i> and <i>UGT1A6</i> polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic children
Zhaosong Du, Hua Xu, Peiwei Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 29, 2021
[Clinical features and genetic analysis of a case with Perlman syndrome due to variant of DIS3L2 gene]
Jing Chen, Chunhui Hu, Lanfen Ren, et al.
Epilepsy Research
|
October 23, 2020
Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic children
Maochang Liu, Junjun Mao, Hua Xu, et al.
Plos One
|
May 13, 2014
Association of mTOR polymorphisms with cancer risk and clinical outcomes: a meta-analysis
Jianbo Shao, Ying Li, Peiwei Zhao, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 30, 2022
Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: Answers
Juanjuan Ding, Panli Liao, Gaohong Zhu, et al.
International Journal of Pediatric Otorhinolaryngology
|
May 6, 2018
2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotonia
Peiwei Zhao, Bing Mao, Xiaonan Cai, et al.
Neurogenetics
|
January 12, 2020
Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams
Peiwei Zhao, Xuehua Peng, Sukun Luo, et al.
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Search research articles
Search
Showing results (1-10 of 42) with videos related to
Sort By:
Page
of 5
Microbiology (Reading, England)
|
August 22, 2009
Identification and characterization of a novel spore-associated subtilase from Thermoactinomyces sp. CDF
Guyue Cheng, Peiwei Zhao, Xiao-Feng Tang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 10, 2018
[Clinical features and genetic analysis of a case with Coffin-Siris syndrome]
Peiwei Zhao, Dan Gao, Yufeng Huang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
February 1, 2019
[Genome-wide copy number microarray analysis for a boy with autism]
Xuelian He, Peiwei Zhao, Yufeng Huang, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems
|
May 18, 2021
Influence of <i>UGT2B7</i> and <i>UGT1A6</i> polymorphisms on plasma concentration to dose ratio of valproic acid in Chinese epileptic children
Zhaosong Du, Hua Xu, Peiwei Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
December 29, 2021
[Clinical features and genetic analysis of a case with Perlman syndrome due to variant of DIS3L2 gene]
Jing Chen, Chunhui Hu, Lanfen Ren, et al.
Epilepsy Research
|
October 23, 2020
Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic children
Maochang Liu, Junjun Mao, Hua Xu, et al.
Plos One
|
May 13, 2014
Association of mTOR polymorphisms with cancer risk and clinical outcomes: a meta-analysis
Jianbo Shao, Ying Li, Peiwei Zhao, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 30, 2022
Gross hematuria, edema, and hypocomplementemia in a 9-year-old boy: Answers
Juanjuan Ding, Panli Liao, Gaohong Zhu, et al.
International Journal of Pediatric Otorhinolaryngology
|
May 6, 2018
2q24 deletion in a 9-month old girl with anal atresia, hearing impairment, and hypotonia
Peiwei Zhao, Bing Mao, Xiaonan Cai, et al.
Neurogenetics
|
January 12, 2020
Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams
Peiwei Zhao, Xuehua Peng, Sukun Luo, et al.
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of 5