Síndrome de Rubinstein-Taybi – FEMEXER

A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot

Rubinstein–Taybi syndrome European Journal of Human Genetics

Quando un WES può indirizzare la clinica: un paziente con sindrome

Sindrome di Rubinstein-Taybi: cos'è e come si manifesta

7 de julio: Día Mundial contra el Síndrome de Rubinstein-Taybi. – Noticias Digital58

PDF] Patent Ductus Arteriousus Device Closure in an Infant with Rubinstein–Taybi Syndrome

Asociación Española Síndrome de Rubinstein Taybi - “La mejor

High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis

Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics

Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect