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CHD7 gene polymorphisms in female patients with idiopathic scoliosis
BACKGROUND: The CHD7 (chromosome domain helicase DNA binding protein 7) gene has been associated with familial idiopathic scoliosis (IS) in families of European descent. The CHD7 single-nucleotide polymorphisms have never been studied in Polish Caucasian IS patients. METHODS: The aim of this study w...
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| Yayımlandı: | BMC Musculoskelet Disord |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6954548/ https://ncbi.nlm.nih.gov/pubmed/31924193 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12891-019-3031-0 |
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