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
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
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
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
Short Report European Journal of Human Genetics
Analysis of mutations within the intron20 splice donor site of CREBBP in  patients with and without classical RSTS
CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
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
PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
Analysis of mutations within the intron20 splice donor site of CREBBP in  patients with and without classical RSTS
Martine J. van Belzen's research works Leiden University Medical Centre, Leiden (LUMC) 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
PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
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