CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder

Congenital glaucoma as a presenting feature of Rubinstein-Taybi

PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome: Deletions associated with polysplenia, hypoplastic left heart and death in infancy

Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

PDF) Identification of a novel de novo mutation of CREBBP in a patient with Rubinstein-Taybi syndrome by targeted next-generation sequencing: A case report

Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

High frequency of copy number imbalances in Rubinstein–Taybi

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP

Expanding the phenotype associated to KMT2A variants: overlapping

Growth charts for individuals with Rubinstein–Taybi syndrome

Chemical and genetic rescue of an ep300 knockdown model for