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Exon deletions of the EP300 and CREBBP genes in two children with

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Exon deletions of the EP300 and CREBBP genes in two children with
Cancers, Free Full-Text
Exon deletions of the EP300 and CREBBP genes in two children with
De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics
Exon deletions of the EP300 and CREBBP genes in two children with
KMT2D acetylation by CREBBP reveals a cooperative functional interaction at enhancers in normal and malignant germinal center B cells
Exon deletions of the EP300 and CREBBP genes in two children with
Mutation spectrum of CREBBP and EP300 in RSTS individuals referenced in
Exon deletions of the EP300 and CREBBP genes in two children with
KMT2D acetylation by CREBBP reveals a cooperative functional interaction at enhancers in normal and malignant germinal center B cells
Exon deletions of the EP300 and CREBBP genes in two children with
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Exon deletions of the EP300 and CREBBP genes in two children with
Genes, Free Full-Text
Exon deletions of the EP300 and CREBBP genes in two children with
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Exon deletions of the EP300 and CREBBP genes in two children with
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Exon deletions of the EP300 and CREBBP genes in two children with
Inactivation of a Single Copy of Crebbp Selectively Alters Pre-mRNA Processing in Mouse Hematopoietic Stem Cells
Exon deletions of the EP300 and CREBBP genes in two children with
Inactivating mutations of acetyltransferase genes in B-cell lymphoma
Exon deletions of the EP300 and CREBBP genes in two children with
RSTS Encyclopedia MDPI
Exon deletions of the EP300 and CREBBP genes in two children with
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
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