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

Rubinstein–Taybi syndrome - Wikipedia

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

Rubinstein-Taybi Syndrome

Rubinstein Taybi syndrome causes, symptoms, diagnosis, treatment & prognosis

Figure 1. [Facial appearance of a girl age 11 years with FHS (SRCAP pathogenic variant p.Arg2444Ter)]. - GeneReviews® - NCBI Bookshelf

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

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

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

Expanding the phenotype associated to KMT2A variants: overlapping

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