Rubinstein–Taybi syndrome: clinical and molecular overview
Por um escritor misterioso
Last updated 01 abril 2025


A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot

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

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

Rubinstein–Taybi syndrome - Wikipedia

CBP Histone Acetyltransferase Activity Regulates Embryonic Neural

A novel mutation c.4003 G>C in the CREBBP gene in an adult female

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

Analysis of mutations within the intron20 splice donor site of

EP300‐related Rubinstein–Taybi syndrome: Highlighted rare

CBP Histone Acetyltransferase Activity Regulates Embryonic Neural
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