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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Exon deletions of the EP300 and CREBBP genes in two children with
IJMS, Free Full-Text
39th Annual David W. Smith Workshop on Malformations and
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Rubinstein‐Taybi syndrome in Chinese population with four novel
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