High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
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The clinical context of copy number variation in the human genome, Expert Reviews in Molecular Medicine
Individual functions of the histone acetyl transferases CBP and p300 in regulating the inflammatory response of synovial fibroblasts - ScienceDirect
PDF) Electroclinical phenotype in Rubinstein–Taybi syndrome
Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization, BMC Genomics
PDF) Mutations in CREBBP and EP300 genes affect DNA repair of oxidative damage in Rubinstein-Taybi syndrome cells
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
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