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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Established and emerging strategies to crack the genetic code of
PDF) Genetic and clinical heterogeneity in Korean patients with
Rubinstein–Taybi syndrome European Journal of Human Genetics
Established and emerging strategies to crack the genetic code of
Identification of the genetic basis of sporadic polydactyly in
IJMS, Free Full-Text
Clinical exome sequencing identifies novel CREBBP variants in 18
IJMS, Free Full-Text
IJMS, Free Full-Text
Rubinstein–Taybi syndrome in diverse populations - Tekendo
Molecular Genetics & Genomic Medicine: Vol 7, No 12
Identification of the genetic basis of sporadic polydactyly in
Further delineation of an entity caused by CREBBP and EP300
High frequency of copy number imbalances in Rubinstein–Taybi
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
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por adulto (o preço varia de acordo com o tamanho do grupo)
