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

Rubinstein–Taybi syndrome - Wikipedia

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

Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

genereviews.org - GeneReviews® - NCBI Bookshelf

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

Beckwith-Wiedemann Syndrome - GeneReviews® - NCBI Bookshelf

Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly

SciELO - Brasil - Prosthetic rehabilitation of a child with Rubinstein-Taybi Syndrome after dental trauma: case report Prosthetic rehabilitation of a child with Rubinstein-Taybi Syndrome after dental trauma: case report

PDF) Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly

Rubinstein-Taybi syndrome with agenesis of corpus callosum