Patient Stories Rubinstein-Taybi Syndrome
Por um escritor misterioso
Last updated 29 dezembro 2024
Children who have Rubinstein-Taybi syndrome can, and do, grow and thrive. Find stories of hope from our patients who are living life to the fullest.
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
Rubinstein-Taybi Syndrome (RTS) Event at the Newport Aquarium – OhioF2F
Rubinstein-Taybi Syndrome: A case report
Forgotten Diseases Research Foundation
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients
The Rubinstein-Taybi Syndrome Children's Foundation
Rubinstein-Taybi Syndrome: A case report
Ultrasound 2-D and 3-D diagnosis of Rubinstein–Taybi syndrome in a 21-week-old fetus
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Learning to Speak at Age 18 with a Sister Who Never Quits (Rubinstein-Taybi Syndrome)
Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly
Rubinstein–Taybi syndrome - Wikipedia
General anesthetic management for dental surgery in an adult patient with Rubinstein-Taybi syndrome, JA Clinical Reports
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