Rubinstein-Taybi syndrome with agenesis of corpus callosum

Forgotten Diseases Research Foundation

Rubinstein-Taybi Syndrome 1

A novel mutation c.4003 G>C in the CREBBP gene in an adult female with Rubinstein–Taybi syndrome presenting with subtle dysmorphic features - Li - 2010 - American Journal of Medical Genetics Part

Cureus Barrett's Esophagus in Rubinstein-Taybi Syndrome

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

Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

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

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

Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes