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Ocular features in Rubinstein-Taybi syndrome: investigation of 24

A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot

Severe persistent pulmonary hypertension in a neonate with

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Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in

Rubinstein–Taybi syndrome European Journal of Human Genetics

RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

High frequency of copy number imbalances in Rubinstein–Taybi

Rubinstein–Taybi syndrome in diverse populations - Tekendo