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
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Descrição
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Rubinstein‐Taybi syndrome in Chinese population with four novel
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein–Taybi syndrome in diverse populations - Tekendo
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