Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
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PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
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A novel CREBBP mutation and its phenotype in a case of Rubinstein
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Genes, Free Full-Text
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PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
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Rubinstein–Taybi syndrome: New neuroradiological and
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Microdeletions and mutations of CREBBP (CBP) gene can cause
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Further delineation of an entity caused by CREBBP and EP300
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome
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Rubinstein–Taybi syndrome - Wikipedia
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EP300‐related Rubinstein–Taybi syndrome: Highlighted rare
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