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8p 11 Microduplication Is Associated with Neonatal Stridor
We report a term male infant with congenital stridor secondary to tracheomalacia and a mild coarctation of the aorta. Developmental delay was noted upon follow-up. Whole genome SNP microarray analysis showed an ∼846-kb interstitial duplication of the short arm of chromosome 8 (8p11.21p11.1). We repo...
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| Vydáno v: | Mol Syndromol |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
S. Karger AG
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6381896/ https://ncbi.nlm.nih.gov/pubmed/30800050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000494796 |
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