Frontiers Case report: A preterm infant with rubinstein-taybi

Exon deletions of the EP300 and CREBBP genes in two children with

A case with Rubinstein-Taybi syndrome: A novel frameshift mutation

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Rubinstein-Taybi Syndrome • RTS Support Group

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What is Rubinstein-Taybi Syndrome? - Goally Apps & Tablets for Kids

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

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Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of

Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect