Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe intellectual disability, distinctive facial features, and broad thumbs and first toes . Explore symptoms, inheritance, genetics of this condition.

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

Rubinstein - Taybi Syndrome (Rubinstein syndrome, broad thumb

New insights into genetic variant spectrum and genotype–phenotype

The behavioral phenotype of Rubinstein–Taybi syndrome: A scoping

PDF) Ocular features in Rubinstein-Taybi syndrome: investigation

Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric

Genes, Free Full-Text

Rubinstein-Taybi syndrome - wikidoc

Empirical Literature on Rubinstein-Taybi Syndrome (RTS) Meeting

Rubinstein-Taybi syndrome: clinical features, genetic basis

Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles

Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein Syndrome - an overview

Identification of de novo EP300 and PLAU variants in a patient

CREBBP mutations in individuals without Rubinstein–Taybi syndrome