中南大学
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返回首页Molecular Subtyping of Autism and Related Neurodevelopmental Disorders We combine medical genetics and clinical phenomics to identify high-risk genes and genotype–phenotype relationships in autism
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We combine medical genetics and clinical phenomics to identify high-risk genes and genotype–phenotype relationships in autism and related neurodevelopmental disorders. By defining molecular subtypes, we aim to establish a scientific basis for precision diagnosis and treatment.