Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Por um escritor misterioso
Descrição
Molecular and genetic dissection of recursive splicing
Graphical representation of the analysis of recursive splicing. Black
PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
Global donor and acceptor splicing site kinetics in human cells
PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
The effect of orientation of the cosmid insert. +, cosmid insert in
Lessons from non-canonical splicing
Classification of reads from the capture dataset mapped to FXR1. For
Combining Engineered U1 snRNA and Antisense Oligonucleotides to Improve the Treatment of a BBS1 Splice Site Mutation: Molecular Therapy - Nucleic Acids
Martijn H Breuning's research works Leiden University Medical Centre, Leiden (LUMC) and other places
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect
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