Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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Graphical representation of the analysis of recursive splicing. Black
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
Short Report European Journal of Human Genetics
CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Arie van Haeringen's research works Leiden University, Leiden (LEI) and other places
PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
Martine J. van Belzen's research works Leiden University Medical Centre, Leiden (LUMC) and other places
Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect
PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
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