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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Detalles Bibliográficos
Autores principales: Shenoy, Rathika Damodara, Shenoy, Vijaya, Shetty, Vikram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Case Report
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

Internet

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

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