Exon deletions of the EP300 and CREBBP genes in two children with
Por um escritor misterioso
Last updated 19 maio 2024
PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch
Human genetics and molecular genomics of Chiari malformation type 1: Trends in Molecular Medicine
Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma - ScienceDirect
Clonal and microclonal mutational heterogeneity in high hyperdiploid acute lymphoblastic leukemia
Inactivating mutations of acetyltransferase genes in B-cell lymphoma
Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma - ScienceDirect
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Localisation of nine CREBBP mutations (six of them of novel
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein–Taybi syndrome detected by aCGH
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Schematic representation of p300 protein and EP300 gene, including
Del Dup And Array - PreventionGenetics
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
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