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A Study on Genetic Polymorphism of RET Proto-Oncogene in Hirschsprung's Disease in Children
BACKGROUND: Hirschsprung's disease (HD) is a genetic disorder with a complex pattern of inheritance. Some single-nucleotide polymorphisms (SNPs) are identified to be associated with the risk of Hirschsprung's Disease (HSCR). AIMS AND OBJECTIVES: The aim of this study is to know the associa...
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| Publicado no: | Afr J Paediatr Surg |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8051638/ https://ncbi.nlm.nih.gov/pubmed/33342844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ajps.AJPS_69_17 |
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