The Ridenour Family - RareKC

A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot

Autism Spectrum Disorder

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

Long-term results following osteotomy of the thumb delta phalanx

Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural

Learning to Speak at Age 18 with a Sister Who Never Quits

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300

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

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

Rubinstein-Taybi syndrome - Atlas of Human Malformation Syndromes in Diverse Populations