Distal 22q11.2 Microduplication
Author:
Affiliation:
1. Division of Pediatric Neurology, Department of Pediatrics, Montreal Children’s Hospital, McGill University Health Centre (MUHC), Montreal, Québec, Canada
2. Department of Medicine, McGill University, Montreal, Québec, Canada
Abstract
Publisher
SAGE Publications
Subject
General Economics, Econometrics and Finance
Link
http://journals.sagepub.com/doi/pdf/10.1177/2329048X17737651
Reference32 articles.
1. A Population-Based Study of the 22q11.2 Deletion: Phenotype, Incidence, and Contribution to Major Birth Defects in the Population
2. Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications
3. A common molecular basis for rearrangement disorders on chromosome 22q11
4. Low copy repeats mediate distal chromosome 22q11.2 deletions: Sequence analysis predicts breakpoint mechanisms
5. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
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