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Our Sub-Departments

Our Sub-departments works on various genomics consltacy services

to provide ealthcare services to patients or human beings with updated technologies in genetics industry. 

Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era

     The identification of gene mutations in syndromic ASDs provided evidence to support a genetic cause of ASDs. 

    Genome-wide copy number variant and sequence analyses have uncovered a list of rare and highly penetrant copy number variants (CNVs) or single nucleotide variants (SNVs) associated with ASDs, which has strengthened the claim of a genetic etiology for ASDs. 

        Findings from research studies in the genetics of ASD now support an important role for molecular diagnostics in the clinical genetics evaluation of ASDs. 

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