Rubinstein-Taybi Syndrome 1

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Last updated 15 abril 2025

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics

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

Rubinstein-Taybi syndrome, medical and dental care for special needs patients: Clinical case report

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

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant

History and Prevalence

The Rubinstein-Taybi Syndrome Children's Foundation

Severe persistent pulmonary hypertension in a neonate with Rubinstein–Taybi syndrome accompanied by triple X syndrome - Pediatrics & Neonatology

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

Rubinstein-Taybi Syndrome 1

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

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