Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis
Zhou, Jinfu, Li, Guilin, Zeng, Yinglin, Qiu, Xiaolong, Zhao, Peiran, Huang, Ting, Wang, Xi, Luo, Jinying, Lin, Na, Xu, Liangpu
Published in Orphanet journal of rare diseases (03.07.2024)
Published in Orphanet journal of rare diseases (03.07.2024)
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Newborn Screening of 6 Lysosomal Storage Disorders by Tandem Mass Spectrometry
Chen, Yao, Yang, Yan, Zeng, Yinglin, Lin, Qingying, Zhao, Peiran, Mao, Bin, Qiu, Xiaolong, Huang, Ting, Xu, Liangpu, Zhu, Wenbin
Published in Clinical pediatrics (01.10.2024)
Published in Clinical pediatrics (01.10.2024)
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Biochemical and molecular features of chinese patients with glutaric acidemia type 1 from Fujian Province, southeastern China
Zhou, Jinfu, Li, Guilin, Deng, Lin, Zhao, Peiran, Zeng, Yinglin, Qiu, Xiaolong, Luo, Jinying, Xu, Liangpu
Published in Orphanet journal of rare diseases (26.07.2023)
Published in Orphanet journal of rare diseases (26.07.2023)
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Biochemical and molecular features of tetrahydrobiopterin deficiency in Fujian Province, southeastern China
Qiu, Xiaolong, Zhao, Peiran, Luo, Jinying, Li, Guilin, Deng, Lin, Zeng, Yinglin, Xu, Liangpu, Zhou, Jinfu
Published in Frontiers in genetics (11.08.2023)
Published in Frontiers in genetics (11.08.2023)
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Screening and the analysis of genotypic and phenotypic characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Fujian province, China
Zhou, Jinfu, Zeng, Yinglin, Tang, Jianping, Chen, Shihong, Li, Guilin, Qiu, Xiaolong, Zhao, Peiran, Huang, Ting, Luo, Jinying, Lin, Na, Xu, Liangpu
Published in Frontiers in genetics (15.07.2024)
Published in Frontiers in genetics (15.07.2024)
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Gene spectrum and clinical traits of 10 patients with primary carnitine deficiency
Chen, Yao, Lin, Qingying, Zeng, Yinglin, Qiu, Xiaolong, Liu, Guanghua, Zhu, Wenbin
Published in Molecular genetics & genomic medicine (01.02.2021)
Published in Molecular genetics & genomic medicine (01.02.2021)
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Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China
Zhou, Jinfu, Zeng, Yinglin, Qiu, Xiaolong, Lin, Qingying, Chen, Weifeng, Luo, Jinying, Xu, Liangpu
Published in Molecular biology reports (01.11.2022)
Published in Molecular biology reports (01.11.2022)
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Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian
Chen, Yao, Lin, Xuehua, Lin, Qingying, Zeng, Yinglin, Qiu, Xiaolong, Liu, Guanghua, Zhu, Wenbin
Published in Medicine (Baltimore) (12.03.2021)
Published in Medicine (Baltimore) (12.03.2021)
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A verification of the application of the non-derivatized mass spectrometry method in newborns screening of metabolic disorders
Zheng, Yulan, Chen, Yao, Qiu, Xiaolong, Chen, Weifen, Lin, Qingying, Zeng, Yinglin, Zhao, Hong, Zhu, Wenbin
Published in Medicine (Baltimore) (01.05.2019)
Published in Medicine (Baltimore) (01.05.2019)
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Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study
Lin, Feng, Chen, Yao, Wang, Jing, Zeng, Yinglin, Chen, Shuwei, Zhu, Wenbin, Yang, Changyi, Zhou, Jinfu, Zhao, Hong
Published in BioMed research international (01.01.2018)
Published in BioMed research international (01.01.2018)
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Mutation of glucose-6-phosphate dehydrogenase deficiency in Chinese Han children in eastern Fujian
Chen, Yao, Xiu, Wenlong, Dong, Yi, Wang, Jing, Zhao, Hong, Su, Yueqing, Zhou, Jinfu, Zeng, Yinglin, Li, Hua, Wo, Jingzhi, Lin, Feng, Zhang, Honghua, Chen, Hanqiang, Yang, Changyi, Zhu, Wenbin
Published in Medicine (Baltimore) (01.07.2018)
Published in Medicine (Baltimore) (01.07.2018)
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Optimized immobilization of activated sludge in poly(ethylene glycol) gels by UV technology
Qiao, Xiangli, Liu, Zhe, Liu, Zhiwei, Zeng, Yinglin, Zhang, Zhenjia
Published in Process biochemistry (1991) (01.08.2010)
Published in Process biochemistry (1991) (01.08.2010)
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Analysis of GCDH gene mutations in 3 patients from Fujian area with glutaric academia type I
Chen, Yao, Lin, Qingying, Zeng, Yinglin, Zhao, Hong, Chen, Weifen, Zhou, Jinfu, Su, Yueqing, Lin, Feng, Zhang, Honghua, Zhu, Wenbin
Published in Zhonghua yi xue yi chuan xue za zhi (10.10.2018)
Published in Zhonghua yi xue yi chuan xue za zhi (10.10.2018)
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Analysis of CYP21A2 gene mutations among patients with classical steroid 21-hydroxylase deficiency
Su, Yueqing, Chen, Hanqiang, Zhu, Wenbin, Wang, Jing, Zhou, Jinfu, Chen, Yao, Zhao, Hong, Zeng, Yinglin, Lin, Feng, Zhang, Honghua, Lin, Qingying
Published in Zhonghua yi xue yi chuan xue za zhi (10.12.2016)
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Published in Zhonghua yi xue yi chuan xue za zhi (10.12.2016)
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