Implications of COMT long-range interactions on the phenotypic variability of 22q11.2 deletion syndrome
Author:
Publisher
Informa UK Limited
Subject
Cell Biology
Link
http://www.tandfonline.com/doi/pdf/10.4161/nucl.27364
Reference38 articles.
1. Genome architecture, rearrangements and genomic disorders
2. Low-Copy Repeats Mediate the Common 3-Mb Deletion in Patients with Velo-cardio-facial Syndrome
3. The 22q11 deletion syndromes
4. Velo-cardio-facial syndrome: 30 Years of study
5. Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
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2. 22q11.2 deletion syndrome: Future directions;The Chromosome 22q11.2 Deletion Syndrome;2022
3. Chromatin Profiling Techniques: Exploring the Chromatin Environment and Its Contributions to Complex Traits;International Journal of Molecular Sciences;2021-07-16
4. Atypical microdeletion 22q11.2 in a patient with tetralogy of Fallot;Journal of Genetics;2021-02-10
5. Identifying of 22q11.2 variations in Chinese patients with development delay;BMC Medical Genomics;2021-01-22
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