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

Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein–Taybi syndrome - Wikipedia

Severe persistent pulmonary hypertension in a neonate with

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

Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect

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

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

Identification of de novo EP300 and PLAU variants in a patient

Approach to inherited hypertrichosis: A brief review - Indian

(PDF) Identification of de novo EP300 and PLAU variants in a