The - The Rubinstein-Taybi Syndrome Children's Foundation
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Last updated 25 março 2025

Rubenstein Taybi Syndrome Oral and Dental Features Carol Mason Consultant in Paediatric Dentistry Great Ormond Street Hospital for Children NHS Foundation. - ppt download

PDF) Rubinstein-Taybi syndrome medical guidelines

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

Genes, Free Full-Text
Our - The Rubinstein-Taybi Syndrome Children's Foundation

Patient Stories Rubinstein-Taybi Syndrome

Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene Mutation

Rubinstein-Taybi Syndrome • RTS Support Group

Logo for Rare Disease Research Foundation by Rtscf

First case of Rubinstein–Taybi syndrome with desquamation associated with a novel mutation in the bromodomain of the CREBBP gene - Wang - 2019 - Clinical and Experimental Dermatology - Wiley Online Library

Special Friends Foundation

Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP

Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
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