Rubinstein–Taybi syndrome European Journal of Human Genetics
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Last updated 17 novembro 2024
Rubinstein-Taybi syndrome, Radiology Reference Article
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly Corresponding author
Rubinstein-Taybi Syndrome
Rubinstein‐Taybi syndrome in Chinese population with four novel mutations - Yu - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
Genes, Free Full-Text
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Cristina Fonseca on LinkedIn: The natural history of adults with Rubinstein-Taybi syndrome: a…
PDF) Rubinstein-Taybi syndrome medical guidelines
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome - JSES International
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome - an overview
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