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Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
PURPOSE: The 1p36 deletion syndrome is a microdeletion syndrome characterized by developmental delays/intellectual disability, craniofacial dysmorphism, and other congenital anomalies. To date, many cases of this syndrome have been reported worldwide. However, cases with this syndrome have not been...
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| Yayımlandı: | Korean J Pediatr |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Korean Pediatric Society
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4753195/ https://ncbi.nlm.nih.gov/pubmed/26893599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3345/kjp.2016.59.1.16 |
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