Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

Forgotten Diseases Research Foundation

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

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

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PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

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

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

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