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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Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
39th Annual David W. Smith Workshop on Malformations and
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
PDF) Identification of the genetic basis of sporadic polydactyly
Clinical exome sequencing identifies novel CREBBP variants in 18
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Established and emerging strategies to crack the genetic code of
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Clinical exome sequencing identifies novel CREBBP variants in 18
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
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