Anaesthetic concerns in an infant with a rare genetic condition; chromosome 9p22 deletion syndrome

Detalles Bibliográficos
Autores principales: Sanket, Bhargavi, Ravindra, Madhavi, Ramavakoda, Chandrika Yabagodu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Letter to Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551034/
https://www.ncbi.nlm.nih.gov/pubmed/26379300
http://dx.doi.org/10.4103/0019-5049.163003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551034/
https://www.ncbi.nlm.nih.gov/pubmed/26379300
http://dx.doi.org/10.4103/0019-5049.163003

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