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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Clinical exome sequencing identifies novel CREBBP variants in 18
Genes, Free Full-Text
Analysis of mutations within the intron20 splice donor site of
IJMS, Free Full-Text
PDF) Genetic and clinical heterogeneity in Korean patients with
IJMS, Free Full-Text
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
High frequency of copy number imbalances in Rubinstein–Taybi
Identification of the genetic basis of sporadic polydactyly in
Identification of the genetic basis of sporadic polydactyly in
Rubinstein‐Taybi syndrome in Chinese population with four novel
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
Case report: a Chinese girl like atypical Rubinstein–Taybi
Molecular Genetics & Genomic Medicine: Vol 7, No 12
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