Rubinstein-Taybi Syndrome - an overview
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a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening
From Diagnosis to Management : Rubinstein – Taybi Syndrome
Rubinstein-Taybi Syndrome 1
Rubinstein taybi syndrome
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
PDF] The behavioural and cognitive phenotype of Rubinstein-Taybi syndrome
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
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