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 28 março 2025
Identification of the genetic basis of sporadic polydactyly in
IJMS, Free Full-Text
Identification of the genetic basis of sporadic polydactyly in
Identification of the genetic basis of sporadic polydactyly in
Rubinstein-Taybi Syndrome - GeneReviews® - NCBI Bookshelf
Rubinstein–Taybi syndrome European Journal of Human Genetics
Rubinstein–Taybi syndrome European Journal of Human Genetics
PDF) Identification of the genetic basis of sporadic polydactyly
PDF) Clinical exome sequencing identifies novel CREBBP variants in
IJMS, Free Full-Text
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Clinical exome sequencing identifies novel CREBBP variants in 18
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