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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | J Clin Diagn Res |
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| Prif Awduron: | , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
JCDR Research and Publications (P) Limited
2015
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| Pynciau: | |
| Mynediad Ar-lein: | 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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