Casarubinstein taybi

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

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Last updated 17 novembro 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
A) Location of the exon CREBBP mutations found in this study. Only
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
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
Mutations and deletions of CREBBP are predominantly monoallelic a, Map
Exon deletions of the EP300 and CREBBP genes in two children with
The missing link between genetic association and regulatory function
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
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Exon deletions of the EP300 and CREBBP genes in two children with
Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers
Exon deletions of the EP300 and CREBBP genes in two children with
Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma - ScienceDirect
Exon deletions of the EP300 and CREBBP genes in two children with
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open
Exon deletions of the EP300 and CREBBP genes in two children with
Childhood Cancer Genomics (PDQ®) - PDQ Cancer Information Summaries - NCBI Bookshelf
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
Chromosome 16p13.3 Deletion Syndrome, Proximal disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Exon deletions of the EP300 and CREBBP genes in two children with
TCF7L2 protein (human) - STRING interaction network
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