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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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Spine Deform
Päätekijät: Gao, Xiaochong, Gotway, Garrett, Rathjen, Karl, Johnston, Charles, Sparagana, Steven, Wise, Carol A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2014
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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