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

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

Floating-Harbor syndrome: MedlinePlus Genetics

Clinical and mutational spectrum in Korean patients with Rubinstein–Taybi syndrome: The spectrum of brain MRI abnormalities - ScienceDirect

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

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

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

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

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

Rubinstein-Taybi syndrome: principal oral and dental disorders and

Frontiers Behavioral and neuropsychiatric challenges across the