Exon deletions of the EP300 and CREBBP genes in two children with
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A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
Inactivating mutations of acetyltransferase genes in B-cell lymphoma
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TCF7L2 protein (human) - STRING interaction network
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
IJMS, Free Full-Text
RSTS Encyclopedia MDPI
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
EP300 Gene - GeneCards, EP300 Protein
De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics
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