Casa
rubinstein taybi omim

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

Por um escritor misterioso

Descrição
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Comprehensive characterisation of intronic mis-splicing mutations in human cancers
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
Martijn H Breuning'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
Volume 24 Issue 11, November 2016
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
Comprehensive characterisation of intronic mis-splicing mutations in human cancers
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Empirical prediction of variant-activated cryptic splice donors using population-based RNA-Seq data
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
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
Systematic Analysis of Splice-Site-Creating Mutations in Cancer - ScienceDirect
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
Therapeutic manipulation of IKBKAP mis-splicing with a small molecule to cure familial dysautonomia
de por adulto (o preço varia de acordo com o tamanho do grupo)