Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients - ScienceDirect

Anaesthesia Management in a Child with Rubinstein - Taybi Syndrome

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

Genes, Free Full-Text

A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring

genereviews.org - GeneReviews® - NCBI Bookshelf

Müllerian Agenesis in a patient with Rubinstein-Taybi Syndrome: A Case Series and Review of the Overlapping Developmental Biologic Pathways - Journal of Pediatric and Adolescent Gynecology

PDF) The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping review of the literature

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

A novel CREBBP mutation and its phenotype in a case of Rubinstein

Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update