Cytogenetic and Clinical Assessment of a Family with Treacher Collins Syndrome

Treacher Collins syndrome (TCS) is a rare autosomal dominant disorder characterized by craniofacial deformities. It is the most common type of mandibulofacial dysostosis (MFD). The objective of this study is to do cytogenetic analysis of a TCS family. Physical examination and all available medical r...

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Detalles Bibliográficos
Autores principales: Kumar, Manoj, Kumar, Rakesh, Tanwar, Mukesh, Ghose, Supriyo, Kaur, Jasbir, Dada, Rima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135159/
https://www.ncbi.nlm.nih.gov/pubmed/21765846
http://dx.doi.org/10.1155/2011/708450

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135159/
https://www.ncbi.nlm.nih.gov/pubmed/21765846
http://dx.doi.org/10.1155/2011/708450

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