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Personalized Medicine|May 20, 2018
Massively parallel sequencing for diagnosing clinically and genetically heterogeneous disordersVictor Wei Zhang
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2012
Determination of the clinical significance of an unclassified variantVictor Wei Zhang, Jing Wang
Biomed Research International|July 3, 2015
Precision Medicine for Continuing Phenotype Expansion of Human Genetic DiseasesHui Yu, Victor Wei Zhang
Molecular Neurobiology|September 7, 2024
A Novel m.1636A > G Variant in Mitochondrial TV Gene Might Cause New Phenotype of Mitochondrial Disease in a 2-Year Old Chinese BoyHaiyan Yang, Victor Wei Zhang, Liang Ai, et al.
Frontiers in Pediatrics|December 5, 2022
Case report: A novel mutation in <i>TRPS</i>1 identified in a Chinese family with tricho-rhino-phalangeal syndrome I: A therapeutic challengeQi Huang, Cheng Jiang, Jiazhong Sun, et al.
International Journal of Laboratory Hematology|January 5, 2021
Identification of thalassemia gene cluster deletion by long-read whole-genome sequencing (LR-WGS)Fan Jiang, Gui-Zhen Lyu, Victor Wei Zhang, et al.
Frontiers in Genetics|March 21, 2024
Identification of a novel <i>KCNT2</i> variant in a family with developmental and epileptic encephalopathies: a case report and literature reviewFengji Cui, Tuoya Wulan, Qian Zhang, et al.
World Journal of Clinical Cases|November 17, 2021
Missense mutation in <i>DYNC1H1</i> gene caused psychomotor developmental delay and muscle weakness: A case reportFeng-Juan Ding, Gui-Zhen Lyu, Victor Wei Zhang, et al.
Frontiers in Neurology|April 18, 2022
Multisystem Mitochondrial Disease Associated With a Mare m.10000G>A Mitochondrial tRNA <sup></sup> (MT-TG) VariantHaiyan Yang, Victor Wei Zhang, Liang Ai, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 5, 2015
Comprehensive Mitochondrial Genome Analysis by Massively Parallel SequencingMeagan E Palculict, Victor Wei Zhang, Lee-Jun Wong, et al.
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