2q31.1 microdeletion syndrome: case report and literature review
Author:
Affiliation:
1. Department of Pediatrics Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.260
Reference14 articles.
1. Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus
2. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: Case report and review
3. Monodactylous Limbs and Abnormal Genitalia Are Associated with Hemizygosity for the Human 2q31 Region That Includes the HOXD Cluster
4. Limb malformations and the humanHOX genes
5. Interstitial deletion of 2q associated with craniosynostosis, ocular coloboma, and limb abnormalities: Cytogenetic and molecular investigation
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