Rubinstein-Taybi Syndrome • RTS Support Group

Rubinstein-Taybi Syndrome (RTS) is an extremely rare genetic condition, occurring in around one person per 125,000 live births.

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes

Anaesthesia Management in a Child with Rubinstein - Taybi Syndrome Scheduled for Punctoplsty, Iranian Journal of Pediatrics

Rubinstein-Taybi Syndrome - an overview

CBP Histone Acetyltransferase Activity Regulates Embryonic Neural Differentiation in the Normal and Rubinstein-Taybi Syndrome Brain: Developmental Cell

Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome

Epigenetic Mechanisms of Rubinstein–Taybi Syndrome

Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are Full of Hope - Global Genes

Psychiatric Profile in Rubinstein-Taybi Syndrome

Rubinstein-Taybi Syndrome • RTS Support Group

Rubinstein–Taybi syndrome - Wikipedia

Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update : Iberoamerican Journal of Medicine : Free Download, Borrow, and Streaming : Internet Archive