Duplication of the ALDH1A2 gene in association with pentalogy of Cantrell: a case report

INTRODUCTION: The pentalogy of Cantrell is rare clustering of congenital defects, first described by Cantrell and colleagues in 1958. The exact pathogenesis for the pentalogy remains unknown and no specific genetic abnormalities have been correlated; however, a failure of embryogenesis has been susp...

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Detalles Bibliográficos
Autores principales: Steiner, Matthew B, Vengoechea, Jaime, Collins, Ronnie Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917519/
https://www.ncbi.nlm.nih.gov/pubmed/24377748
http://dx.doi.org/10.1186/1752-1947-7-287

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917519/
https://www.ncbi.nlm.nih.gov/pubmed/24377748
http://dx.doi.org/10.1186/1752-1947-7-287

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