Rubinstein-Taybi syndrome with agenesis of corpus callosum

Rubinstein-Taybi syndrome: MedlinePlus Genetics

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Rubinstein Taybi Syndrome: Most Up-to-Date Encyclopedia, News & Reviews

Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf

The novel and recurrent variants in exon 31 of CREBBP in Japanese patients with Menke–Hennekam syndrome - Nishi - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library

Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature

Cureus, Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7

Rubinstein-Taybi syndrome (RTS)

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome