Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome: clinical features, genetic basis
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Congenital basis of posterior fossa anomalies. - Abstract - Europe PMC
Genes, Free Full-Text
Facial dysmorphism, skeletal anomalies, congenital glucoma
Rubinstein–Taybi syndrome: New neuroradiological and
Cerebellar hypoplasia, dysplasia, and enlargement
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