Rubinstein–Taybi syndrome - Wikipedia

Forgotten Diseases Research Foundation

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

Congenital glaucoma as a presenting feature of Rubinstein-Taybi

PDF) Rubinstein-Taybi syndrome medical guidelines

Clinical and molecular findings of the six patients with Rubinstein

Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein- Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia – topic of research paper in Clinical medicine. Download scholarly article PDF

Main clinical findings of the 16 Brazilian patients with

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

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

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP