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Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes
BACKGROUND: Genome-wide association studies have identified associations of genetic variants at 17q21 near ORMDL3 with childhood asthma. OBJECTIVES: To find out whether associations in this region are specific to particular asthma phenotypes and specific to ORMDL3. METHODS: We examined associations...
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| Yayımlandı: | J Allergy Clin Immunol |
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| Asıl Yazarlar: | , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4427593/ https://ncbi.nlm.nih.gov/pubmed/23154084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2012.09.021 |
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