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 16 setembro 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
IJMS, Free Full-Text
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
Established and emerging strategies to crack the genetic code of
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
Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
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 a Saudi boy with distinct features
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
Molecular Genetics & Genomic Medicine: Vol 7, No 12
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
IJMS, Free Full-Text
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
Analysis of mutations within the intron20 splice donor site of
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
PDF) Genetic and clinical heterogeneity in Korean patients with
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
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with
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

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