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  1. 1
    Intellectual developmental disorder with cardiac arrhythmia syndrome in a family caused by GNB5 variation and literature review

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  2. 2
    A family with Allan-Herndon-Dudley syndrome due to SLC16A2 gene mutation

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  3. 3
    Clinical and laboratory characteristics and genetic diagnosis of Kabuki syndrome

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  4. 4
    A novel mutation in KCNB1 gene in a child with neuropsychiatric comorbidities with both intellectual disability and epilepsy and review of literature

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  5. 5
    Clinical manifestation and gene analyses of 15 patients with intellectual disability or developmental delay complicated with congenital nystagmus

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