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Genomic analyses of patients with unexplained early onset scoliosis
STUDY DESIGN: To test for rare genetic mutations, a cohort of patients with unexplained early onset scoliosis (EOS) was screened using high-density microarray genotyping. A cohort of patients with adolescent idiopathic scoliosis (AIS) was similarly screened, and the results were compared. SUMMARY OF...
Tallennettuna:
| Julkaisussa: | Spine Deform |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4228381/ https://ncbi.nlm.nih.gov/pubmed/27927329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jspd.2014.04.014 |
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