Broad thumbs and broad hallux: the hallmarks for the Rubinstein

Forgotten Diseases Research Foundation

Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP

Rubinstein Taybi Syndrome Awareness RTS Hearts and

Clinical photos of the patients. (a) Case 1: Dysmorphic facial

Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene

4 Newborn with Rubinstein-Taybi syndrome showing microcephaly

SciELO - Brasil - Multiple pilomatricomas in twins with Rubinstein

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

A novel CREBBP mutation and its phenotype in a case of Rubinstein

Rubinstein-Taybi syndrome in a Saudi boy with distinct features