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 Chinese  Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu -  2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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
Clinical exome sequencing identifies novel CREBBP variants in 18
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
Clinical exome sequencing identifies novel CREBBP variants in 18
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
First case of Rubinstein–Taybi syndrome with desquamation
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
Identification of the genetic basis of sporadic polydactyly in
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 Chinese  Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu -  2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Rubinstein–Taybi syndrome in diverse populations - Tekendo
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
Clinical exome sequencing identifies novel CREBBP variants in 18
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
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
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
Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
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
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With

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