Congenital glaucoma as a presenting feature of Rubinstein-Taybi

Genes, Free Full-Text

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

PDF) Rubinstein-Taybi syndrome medical guidelines

PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

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

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

Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Main clinical findings of the 16 Brazilian patients with

Rubinstein-Taybi syndrome in a Saudi boy with distinct features