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

Rubinstein-Taybi syndrome: Dental manifestations and management

Figure 2. [Dorsal (A) and palmar (B)]. - 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

Genes, Free Full-Text

The novel and recurrent variants in exon 31 of CREBBP in Japanese patients with Menke–Hennekam syndrome - Nishi - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library

Beckwith-Wiedemann Syndrome - GeneReviews® - NCBI Bookshelf

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

Rubinstein–Taybi syndrome in diverse populations - Tekendo

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

Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology