Associated Papers
Novel TBR1 c.1303C>T Variant Led to Diagnosis of Intellectual Developmental Disorder with Autism and Speech Delay: Application of Comprehensive Family-Based Whole-Genome Analysis.
Ćuk M et al.
Genes, 2025
Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability.
Jin C et al.
Taiwanese Journal of Obstetrics & Gynecology, 2021
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