Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
Por um escritor misterioso
Last updated 02 abril 2025


Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome

Rubinstein-Taybi Syndrome

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Microdeletions and mutations of CREBBP (CBP) gene can cause

Rubinstein-Taybi Syndrome – New Indian Journal of Pediatrics

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Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

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Rubinstein-Taybi Syndrome

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein–Taybi and Filippi syndromes

Rubinstein-Taybi Syndrome: A Female Patient with a De Novo Reciprocal Translocation T(2; 16)(Q36.3; P13.3) and Dysgranulopoiesis

Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS

Rubinstein-Taybi syndrome: MedlinePlus Genetics
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