Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe intellectual disability, distinctive facial features, and broad thumbs and first toes . Explore symptoms, inheritance, genetics of this condition.

PDF) Ocular features in Rubinstein-Taybi syndrome: investigation

Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein

Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment

Rubinstein-Taybi Syndrome by Alexandra Wilegus

BJORL - Brazilian Journal of Otorhinolaryngology

Frontiers Behavioral and neuropsychiatric challenges across the

Frontiers Behavioral and neuropsychiatric challenges across the

Canal Dehiscense

New insights into genetic variant spectrum and genotype–phenotype

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

PDF] Rubinstein-Taybi syndrome. Review of 732 cases and analysis

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Rubinstein-Taybi Syndrome: Genetics

Rubinstein–Taybi syndrome: clinical and molecular overview