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Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS

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Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Research articles European Journal of Human Genetics
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Combining Engineered U1 snRNA and Antisense Oligonucleotides to Improve the Treatment of a BBS1 Splice Site Mutation: Molecular Therapy - Nucleic Acids
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Otopalatodigital Syndrome, Type Ii disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Arie van Haeringen's research works Leiden University, Leiden (LEI) and other places
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Arie van Haeringen's research works Leiden University, Leiden (LEI) and other places
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Molecular and genetic dissection of recursive splicing
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Rahikkala ELISA, Oulu University Hospital, Oulu, Department of Clinical Genetics
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Characterization of splice-altering mutations in inherited predisposition to cancer
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Graphical representation of the analysis of recursive splicing. Black
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Classification of reads from the capture dataset mapped to FXR1. For
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
CREBBP/EP300 mutations promoted tumor progression in diffuse large B-cell lymphoma through altering tumor-associated macrophage polarization via FBXW7-NOTCH-CCL2/CSF1 axis
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