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

Clinical exome sequencing identifies novel CREBBP variants in 18

Rubinstein‐Taybi syndrome in Chinese population with four novel

Molecular Genetics & Genomic Medicine: Vol 7, No 12

Molecular Genetics & Genomic Medicine: Vol 7, No 12

Identification of the genetic basis of sporadic polydactyly in

Identification of the genetic basis of sporadic polydactyly in

Identification of the genetic basis of sporadic polydactyly in

Clinical exome sequencing identifies novel CREBBP variants in 18

Further delineation of an entity caused by CREBBP and EP300

Rubinstein–Taybi syndrome in diverse populations - Tekendo