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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...
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| Publicat a: | Case Rep Genet |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6151207/ https://ncbi.nlm.nih.gov/pubmed/30271639 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/1928918 |
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