Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Por um escritor misterioso
Last updated 19 setembro 2024
Empirical prediction of variant-activated cryptic splice donors using population-based RNA-Seq data
Characterization of splice-altering mutations in inherited predisposition to cancer
Classification of the paired-end reads. (A) 'Mapping distance' reflects
Systematic Analysis of Splice-Site-Creating Mutations in Cancer - ScienceDirect
Evolution of the U2 Spliceosome for Processing Numerous and Highly Diverse Non-canonical Introns in the Chordate Fritillaria borealis - ScienceDirect
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect
Splicing mutations in human genetic disorders: examples, detection, and confirmation
Splice-Site Mutations: A Novel Genetic Mechanism of Crigler-Najjar Syndrome Type 1 - ScienceDirect
The effect of orientation of the cosmid insert. +, cosmid insert in
Principles of the two approaches to investigate non-sequential
The effect of orientation of the cosmid insert. +, cosmid insert in
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