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Publications by Wenjia Tong
Whole-Exome Sequencing Helps the Diagnosis and Treatment in Children With Neurodevelopmental Delay Accompanied Unexplained Dyspnea
Scientific Reports
Multidisciplinary
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Application of Whole Exome Sequencing in the Diagnosis of Hereditary Neurological Diseases
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Whole Exome Sequencing in Monogenic Dyslipidemias
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Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
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P05.10: Using Whole-Exome Sequencing in Prenatal Diagnosis of Severe Fetal Abnormalities
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A De Novo Heterozygous Frameshift Mutation Identified in BCL11B Causes Neurodevelopmental Disorder by Whole Exome Sequencing
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125: Whole Exome Sequencing (WES) in Prenatal Diagnosis for Carefully Selected Cases
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Effectiveness of Whole-Exome Sequencing and Costs of the Traditional Diagnostic Trajectory in Children With Intellectual Disability
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Clinical Application of Whole-Exome Sequencing
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