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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Last updated 21 outubro 2024
Clinical exome sequencing identifies novel CREBBP variants in 18
Clinical exome sequencing identifies novel CREBBP variants in 18
First case of Rubinstein–Taybi syndrome with desquamation
Identification of the genetic basis of sporadic polydactyly in
IJMS, Free Full-Text
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Clinical exome sequencing identifies novel CREBBP variants in 18
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
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