Silver Russell Syndrome: Most Up-to-Date Encyclopedia, News & Reviews

Forgotten Diseases Research Foundation

Rubinstein Taybi syndrome causes, symptoms, diagnosis, treatment & prognosis

A novel mutation c.4003 G>C in the CREBBP gene in an adult female with Rubinstein–Taybi syndrome presenting with subtle dysmorphic features - Li - 2010 - American Journal of Medical Genetics Part

Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf

PDF) The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping review of the literature

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Rubinstein-Taybi syndrome with agenesis of corpus callosum. - Abstract - Europe PMC

Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology

(PDF) Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly

Rubinstein-Taybi syndrome with agenesis of corpus callosum