Casarubinstein taybi

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

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Last updated 15 junho 2024
Exon deletions of the EP300 and CREBBP genes in two children with
Exon deletions of the EP300 and CREBBP genes in two children with
CREBBP/EP300 mutations promoted tumor progression in diffuse large B-cell lymphoma through altering tumor-associated macrophage polarization via FBXW7-NOTCH-CCL2/CSF1 axis
Exon deletions of the EP300 and CREBBP genes in two children with
Human genetics and molecular genomics of Chiari malformation type 1: Trends in Molecular Medicine
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
From Whole Gene Deletion to Point Mutations of EP300‐Positive Rubinstein–Taybi Patients: New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks - Negri - 2016 - Human Mutation - Wiley Online Library
Exon deletions of the EP300 and CREBBP genes in two children with
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
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
EP300 Gene - GeneCards, EP300 Protein
Exon deletions of the EP300 and CREBBP genes in two children with
CREBBP (CREB binding protein)
Exon deletions of the EP300 and CREBBP genes in two children with
TCF7L2 protein (human) - STRING interaction network
Exon deletions of the EP300 and CREBBP genes in two children with
Del Dup And Array - PreventionGenetics
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
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
Exon deletions of the EP300 and CREBBP genes in two children with
Clinical and molecular characteristics of MEF2D fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in MEF2D-HNRNPH1 gene fusion
Exon deletions of the EP300 and CREBBP genes in two children with
Novel heterozygous variants in the EP300 gene cause Rubinstein–Taybi syndrome 2: Reports from two Chinese children - Du - 2023 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Exon deletions of the EP300 and CREBBP genes in two children with
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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