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A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome
We report a 14-year-old Hispanic male with a microduplication of the chromosome 7p22.2 band detected through microarray analysis. He had a history of developmental delay and mild intellectual disability, asthma, myopia, proportionate short stature, dysmorphic features, and Achilles tendon release. T...
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| Yayımlandı: | J Pediatr Genet |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Georg Thieme Verlag KG
2015
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| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4906420/ https://ncbi.nlm.nih.gov/pubmed/27617114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0035-1554980 |
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