Rubinstein-Taybi Syndrome - an overview

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117 out of

PDF) Oro-dental features as useful diagnostic tool in Rubinstein–Taybi syndrome

Case report: a Chinese girl like atypical Rubinstein–Taybi syndrome caused by a novel heterozygous mutation of the EP300 gene, BMC Medical Genomics

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

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

Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

High frequency of copy number imbalances in Rubinstein–Taybi

Rubinstein‐Taybi syndrome in Chinese population with four novel