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Frontiers in Genetics|July 23, 2025
Correction: A non-invasive method for screening mitochondrial diabetesHangyu Fang, Xiaoe Li, Shuping Wang, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|October 5, 2022
Identification of TUBB8 Variants in 5 Primary Infertile Women with Multiple Phenotypes in Oocytes and Early EmbryosWenzhu Yu, Shaodi Zhang, Baoli Yin, et al.
The International Journal of Neuroscience|March 18, 2014
Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 geneAziz Shaibani, Lee-Jun Wong, Victor Wei Zhang, et al.
BMC Pediatrics|October 23, 2019
Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness - a case report for dual diagnosisYan Zhang, Yi Zhang, Victor Wei Zhang, et al.
Cytogenetic and Genome Research|March 9, 2023
Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome SequencingJuan Chen, Gui-Zhen Lyu, Fan Jiang, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A <i>SUCLG1</i> 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 <i>AGK</i> 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.
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.
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.
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