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 fevereiro 2025
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Rubinstein–Taybi syndrome in diverse populations - Tekendo
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Molecular analysis of the CBP gene in 60 patients with Rubinstein
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Established and emerging strategies to crack the genetic code of
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Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
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PDF) Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel
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Identification of the genetic basis of sporadic polydactyly in
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Rubinstein–Taybi syndrome in diverse populations - Tekendo
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IJMS, Free Full-Text
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Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
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Identification of the genetic basis of sporadic polydactyly in

PDF) Identification of the genetic basis of sporadic polydactyly
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Rubinstein–Taybi syndrome in diverse populations - Tekendo
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