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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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Detalhes bibliográficos
Main Authors: Kumar, Manoj, Kumar, Rakesh, Tanwar, Mukesh, Ghose, Supriyo, Kaur, Jasbir, Dada, Rima
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3135159/
https://ncbi.nlm.nih.gov/pubmed/21765846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/708450
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