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

Identification of the genetic basis of sporadic polydactyly in

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Identification of the genetic basis of sporadic polydactyly in

Identification of the genetic basis of sporadic polydactyly in

Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf

Rubinstein–Taybi syndrome European Journal of Human Genetics

Rubinstein–Taybi syndrome European Journal of Human Genetics

PDF) Identification of the genetic basis of sporadic polydactyly

PDF) Clinical exome sequencing identifies novel CREBBP variants in

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Molecular Genetics & Genomic Medicine: Vol 7, No 12

Clinical exome sequencing identifies novel CREBBP variants in 18