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Molecular Genetics and Metabolism Reports|November 30, 2016
A SUCLG1 mutation in a patient with mitochondrial DNA depletion and congenital anomaliesMegan L Landsverk, Victor Wei Zhang, Lee-Jun C Wong, et al.
Frontiers in Pediatrics|June 24, 2021
Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK GeneBenzhen Wang, Zhanhui Du, Guangsong Shan, et al.
Frontiers in Genetics|June 16, 2025
A non-invasive method for screening mitochondrial diabetesHangyu Fang, Xiaoe Li, Shuping Wang, et al.
Waste Management (New York, N.Y.)|February 12, 2022
Co-pyrolysis of sewage sludge and food waste digestate to synergistically improve biochar characteristics and heavy metals immobilizationXingdong Wang, Victor Wei-Chung Chang, Zhiwei Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2014
Improved molecular diagnosis by the detection of exonic deletions with target gene capture and deep sequencingYanming Feng, David Chen, Guo-Li Wang, et al.
BMC Palliative Care|January 24, 2026
Tree of peaches: exploring what matters most at the end-of-life among healthy older adults in Taiwan: a qualitative studyVictor Wei-Che Shen, Wei-Chi V Shen, Ernest Wen-Ruey Yu, et al.
Frontiers in Genetics|March 25, 2025
Application of rapid clinical exome sequencing technology in the diagnosis of critically ill pediatric patients with suspected genetic diseasesXuejun Ouyang, Yu Zhang, Tian Yu, et al.
Plos One|October 13, 2017
DNA accumulation on ventilation system filters in university buildings in SingaporeIrvan Luhung, Yan Wu, Siyu Xu, et al.
Hemoglobin|November 30, 2018
A Rare Hb H Hydrops Fetalis Syndrome Caused by the - -SEA Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese PatientQiang Li, Yihong Li, Mei Zhong, et al.
Frontiers in Neurology|May 21, 2020
Identification and Clinical Analysis of the First Nonsense Mutation in the PSEN1 Gene in a Family With Acute Encephalopathy and Retinitis PigmentosaChunlin You, Weike Zeng, Lingna Deng, et al.
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