Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
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Classification of the paired-end reads. (A) 'Mapping distance' reflects

Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect

CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library

Martine J. van Belzen's research works Leiden University Medical Centre, Leiden (LUMC) and other places

PDF) Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome

Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect

Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect

PDF) Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome

Research articles European Journal of Human Genetics

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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

CREBBP/EP300 mutations promoted tumor progression in diffuse large B-cell lymphoma through altering tumor-associated macrophage polarization via FBXW7-NOTCH-CCL2/CSF1 axis

Exploration of Coding and Non-coding Variants in Cancer Using GenomePaint - ScienceDirect
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