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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Identification of the genetic basis of sporadic polydactyly in
Identification of the genetic basis of sporadic polydactyly in
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Established and emerging strategies to crack the genetic code of
Clinical exome sequencing identifies novel CREBBP variants in 18
Rubinstein–Taybi syndrome European Journal of Human Genetics
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Clinical exome sequencing identifies novel CREBBP variants in 18
Identification of the genetic basis of sporadic polydactyly in
Exon deletions of the EP300 and CREBBP genes in two children with
Rubinstein–Taybi syndrome European Journal of Human Genetics
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Exon deletions of the EP300 and CREBBP genes in two children with
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Rubinstein–Taybi syndrome European Journal of Human Genetics
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