The human brain and face: mechanisms of cranial, neurological and facial development revealed through malformations of holoprosencephaly, cyclopia and aberrations in chromosome 18

The study of inborn genetic errors can lend insight into mechanisms of normal human development and congenital malformations. Here, we present the first detailed comparison of cranial and neuro pathology in two exceedingly rare human individuals with cyclopia and alobar holoprosencephaly (HPE) in th...

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Detalhes bibliográficos
Publicado no:J Anat
Main Authors: Gondré-Lewis, Marjorie C, Gboluaje, Temitayo, Reid, Shaina N, Lin, Stephen, Wang, Paul, Green, William, Diogo, Rui, Fidélia-Lambert, Marie N, Herman, Mary M
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2015
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4560560/
https://ncbi.nlm.nih.gov/pubmed/26278930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/joa.12343
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