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Orofacial Manifestations of Autosomal Recessive Robinow’s Syndrome: A Rare Case Report

Robinow’s syndrome is a very rare genetic disorder which bears a resemblance to a foetal face. It is characterized by short-limbed dwarfism, defects in vertebral segmentation and abnormalities in the head, face and external genitalia. It has a genetic heterogeneity with autosomal dominant and recess...

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Detalhes bibliográficos
Publicado no:J Clin Diagn Res
Main Authors: Mali, Santosh, Bansal, Neha, Dhokar, Amol, Yadav, Monica
Formato: Artigo
Idioma:Inglês
Publicado em: JCDR Research and Publications (P) Limited 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4843398/
https://ncbi.nlm.nih.gov/pubmed/27135013
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2016/16318.7469
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