Casarubinstein síndrome

Rubinstein–Taybi syndrome European Journal of Human Genetics

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Last updated 15 novembro 2024
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein–Taybi syndrome European Journal of Human Genetics
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Rubinstein–Taybi syndrome European Journal of Human Genetics
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein–Taybi syndrome European Journal of Human Genetics
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 European Journal of Human Genetics
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome / X
Rubinstein–Taybi syndrome European Journal of Human Genetics
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Rubinstein–Taybi syndrome European Journal of Human Genetics
Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
Rubinstein–Taybi syndrome European Journal of Human Genetics
Dandy walker variant an association with Rubinstein Taybi syndrome
Rubinstein–Taybi syndrome European Journal of Human Genetics
Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly
Rubinstein–Taybi syndrome European Journal of Human Genetics
PDF) Genetic heterogeneity in Rubinstein-Taybi syndrome: Delineation of the phenotype of the first patients carrying mutations in EP300
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein-Taybi Syndrome
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