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Frontiers in Public Health
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October 15, 2024
Improved staffing policies and practices in healthcare based on a conceptual model
Ning Wei, Zhongwei Wang, Xiyuan Li, et al.
Brain & Development
|
April 9, 2015
Five Chinese patients with 5-oxoprolinuria due to glutathione synthetase and 5-oxoprolinase deficiencies
Xiyuan Li, Yuan Ding, Yupeng Liu, et al.
European Journal of Medical Genetics
|
February 6, 2015
Very long-chain acyl-coenzyme A dehydrogenase deficiency in Chinese patients: eight case reports, including one case of prenatal diagnosis
Xiyuan Li, Yuan Ding, Yanyan Ma, et al.
Journal of Human Genetics
|
October 21, 2016
Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome
Bing Xu, Xiyuan Li, Miaomiao Du, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 3, 2020
Identification of a novel homozygous nonsense variant in a Chinese patient with ethylmalonic encephalopathy and a genotype-phenotype spectrum review
Yilun Tao, Dong Han, Xiyuan Li, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
September 12, 2013
[HEXB gene study and prenatal diagnosis for a family affected by infantile Sandhoff disease]
Tongfei Wu, Xiyuan Li, Qiao Wang, et al.
Applied Optics
|
March 17, 2026
Quantitative correlation between surface defect dimensions and absorption in optical components
Fengwei Zhang, Xiongtao Lv, Shaowen Wang, et al.
European Journal of Medical Genetics
|
September 18, 2017
A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2
Dongxiao Li, Hui Dong, Hong Zheng, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
September 6, 2014
[Clinical and laboratory studies on 28 patients with glutaric aciduria type 1]
Qiao Wang, Yuan Ding, Yupeng Liu, et al.
The Journal of Craniofacial Surgery
|
September 2, 2022
Bioinformatics Analysis of Hub Genes Involved in Alcohol-Related Hemifacial Microsomia Pathogenesis
Lunkun Ma, Shanbaga Zhao, Xi Xu, et al.
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Search research articles
Search
Showing results (31-40 of 88) with videos related to
Sort By:
Page
of 9
Frontiers in Public Health
|
October 15, 2024
Improved staffing policies and practices in healthcare based on a conceptual model
Ning Wei, Zhongwei Wang, Xiyuan Li, et al.
Brain & Development
|
April 9, 2015
Five Chinese patients with 5-oxoprolinuria due to glutathione synthetase and 5-oxoprolinase deficiencies
Xiyuan Li, Yuan Ding, Yupeng Liu, et al.
European Journal of Medical Genetics
|
February 6, 2015
Very long-chain acyl-coenzyme A dehydrogenase deficiency in Chinese patients: eight case reports, including one case of prenatal diagnosis
Xiyuan Li, Yuan Ding, Yanyan Ma, et al.
Journal of Human Genetics
|
October 21, 2016
Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome
Bing Xu, Xiyuan Li, Miaomiao Du, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 3, 2020
Identification of a novel homozygous nonsense variant in a Chinese patient with ethylmalonic encephalopathy and a genotype-phenotype spectrum review
Yilun Tao, Dong Han, Xiyuan Li, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
September 12, 2013
[HEXB gene study and prenatal diagnosis for a family affected by infantile Sandhoff disease]
Tongfei Wu, Xiyuan Li, Qiao Wang, et al.
Applied Optics
|
March 17, 2026
Quantitative correlation between surface defect dimensions and absorption in optical components
Fengwei Zhang, Xiongtao Lv, Shaowen Wang, et al.
European Journal of Medical Genetics
|
September 18, 2017
A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2
Dongxiao Li, Hui Dong, Hong Zheng, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics
|
September 6, 2014
[Clinical and laboratory studies on 28 patients with glutaric aciduria type 1]
Qiao Wang, Yuan Ding, Yupeng Liu, et al.
The Journal of Craniofacial Surgery
|
September 2, 2022
Bioinformatics Analysis of Hub Genes Involved in Alcohol-Related Hemifacial Microsomia Pathogenesis
Lunkun Ma, Shanbaga Zhao, Xi Xu, et al.
Page
of 9