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.

Epigenetic diseases and their causes and symptoms.

Rubinstein-Taybi syndrome: MedlinePlus Genetics

Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein

First case report of inherited Rubinstein-Taybi syndrome

Chromosome 16: MedlinePlus Genetics

Epigenetic Mechanisms of Rubinstein–Taybi Syndrome

The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping

Rubinstein–Taybi syndrome European Journal of Human Genetics

IJMS, Free Full-Text

Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in

Rubinstein–Taybi syndrome: clinical and molecular overview

Empirical Literature on Rubinstein-Taybi Syndrome (RTS) Meeting