Chemical and genetic rescue of an ep300 knockdown model for

Rubinstein–Taybi syndrome - Wikipedia

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

Rubinstein-Taybi syndrome: Dental manifestations and management

Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire

Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome

Two adults with Rubinstein–Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers - Wieczorek - 2009 - American Journal of Medical Genetics Part A

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

High frequency of copy number imbalances in Rubinstein–Taybi