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De novo triplication of 11q12.3 in a patient with developmental delay and distinctive facial features
BACKGROUND: Triplication is a rare chromosomal anomaly. We identified a de novo triplication of 11q12.3 in a patient with developmental delay, distinctive facial features, and others. In the present study, we discuss the mechanism of triplications that are not embedded within duplications and potent...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3626894/ https://ncbi.nlm.nih.gov/pubmed/23552394 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-6-15 |
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