Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
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Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Rubinstein-Taybi Syndrome: A Case Report
PDF] Rubinstein-Taybi Syndrome in a 19-years old boy.
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly
Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
PDF) Rubinstein-Taybi syndrome: A case report
An unusual presentation of Rubinstein-Taybi Syndrome with bilateral postaxial polydactyly
Novel heterozygous variants in the EP300 gene cause Rubinstein–Taybi syndrome 2: Reports from two Chinese children - Du - 2023 - Molecular Genetics & Genomic Medicine - Wiley Online Library
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis, diagnosis, and management
PDF) Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature
DBMCI MDS : Formerly MDS Experts - RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: - Mental retardation - Broad thumbs
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