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Chromosomal Abnormalities in Syndromic Orofacial Clefts: Report of Three Children
This case series of three children reports clinical features and chromosomal abnormalities seen in a craniofacial clinic. All presented with orofacial cleft, developmental or intellectual disability, and dysmorphism. Emanuel syndrome or supernumerary der (22)t(11; 22), the prototype of complex small...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Hindawi
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151207/ https://www.ncbi.nlm.nih.gov/pubmed/30271639 http://dx.doi.org/10.1155/2018/1928918 |