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
New insights into genetic variant spectrum and genotype–phenotype
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
Case report: a Chinese girl like atypical Rubinstein–Taybi
Molecular Genetics & Genomic Medicine: Vol 7, No 12
High frequency of copy number imbalances in Rubinstein–Taybi
IJMS, Free Full-Text
IJMS, Free Full-Text
PDF) Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel
Molecular analysis of the CBP gene in 60 patients with Rubinstein
Rubinstein‐Taybi syndrome in Chinese population with four novel
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
Genes, Free Full-Text
First case of Rubinstein–Taybi syndrome with desquamation
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por adulto (o preço varia de acordo com o tamanho do grupo)
