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Hirschsprung’s Disease in Neonates with Special Reference to Calretinin Immunohistochemistry
BACKGROUND: Hirschsprung’s disease is a classic example of a complex genetic disease, characterized by the lack of enteric ganglia in the submucosal and myenteric plexuses, along variable portions of the distal gut. The diagnosis of Hirschsprung’s disease is based on a combination of clinical featur...
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| Publicat a: | J Clin Diagn Res |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
JCDR Research and Publications (P) Limited
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4572963/ https://ncbi.nlm.nih.gov/pubmed/26417550 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2015/12470.6180 |
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