{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,28]],"date-time":"2026-03-28T02:25:45Z","timestamp":1774664745078,"version":"3.50.1"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"10","content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2014,10]]},"DOI":"10.1007\/s11999-014-3766-8","type":"journal-article","created":{"date-parts":[[2014,7,8]],"date-time":"2014-07-08T14:26:57Z","timestamp":1404829617000},"page":"3216-3225","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":20,"title":["Are Copy Number Variants Associated With Adolescent Idiopathic Scoliosis?"],"prefix":"10.1097","volume":"472","author":[{"given":"Jillian G.","family":"Buchan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David M.","family":"Alvarado","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gabe","family":"Haller","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hyuliya","family":"Aferol","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nancy H.","family":"Miller","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Matthew B.","family":"Dobbs","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christina A.","family":"Gurnett","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R8-43-20210317","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1016\/j.ejmg.2009.03.006","article-title":"Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.","volume":"52","author":"Bijlsma","year":"2009","journal-title":"Eur J Med Genet"},{"key":"R12-43-20210317","first-page":"261","article-title":"Outline for the study of scoliosis.","volume":"5","author":"Cobb","year":"1948","journal-title":"Instr Course Lect"},{"key":"R18-43-20210317","first-page":"5646","article-title":"Triple X syndrome deviation with mild symptoms: the majority goes undiagnosedin Swedish.","volume":"96","author":"Gustavson","year":"1999","journal-title":"Lakartidningen"},{"key":"R26-43-20210317","first-page":"2898","article-title":"The pathogenesis of adolescent idiopathic scoliosis: review of the literature. Spine (Phila Pa 1976).","volume":"33","author":"Kouwenhoven","year":"2008","journal-title":""},{"key":"R31-43-20210317","first-page":"619","article-title":"Linden, MG., Bender, BG., Harmon, RJ., Mrazek, DA. and Robinson, A.47, XXX: what is the prognosis?","volume":"82","year":"1988","journal-title":"Pediatrics"},{"issue":"Database issue","key":"R32-43-20210317","doi-asserted-by":"crossref","first-page":"D986","DOI":"10.1093\/nar\/gkt958","article-title":"The Database of Genomic Variants: a curated collection of structural variation in the human genome.","volume":"42","author":"MacDonald","year":"2014","journal-title":"Nucleic Acids Res"},{"key":"R43-43-20210317","first-page":"111","article-title":"Reamy, BV. and Slakey, JB. Adolescent idiopathic scoliosis: review and current concepts.","volume":"64","year":"2001","journal-title":"Am Fam Physician"},{"key":"R44-43-20210317","doi-asserted-by":"crossref","first-page":"974","DOI":"10.2106\/00004623-197355050-00006","article-title":"Riseborough, EJ. and Wynne-Davies, R. A genetic survey of idiopathic scoliosis in Boston, Massachusetts.","volume":"55","year":"1973","journal-title":"J Bone Joint Surg Am"},{"key":"R50-43-20210317","doi-asserted-by":"crossref","first-page":"e727","DOI":"10.1542\/peds.2009-1684","article-title":"3rd, Lincoln SA, Lowe KR, Schonwald A, Robbins M, Hisama F, Wolff R, Becker R, Nasir R, Urion DK, Milunsky JM, Rappaport L, Gusella JF, Walsh CA, Wu BL, Miller DT, Autism Consortium Clinical GeneticsDNA Diagnostics Collaboration. Clinical genetic testing for patients with autism spectrum disorders.","volume":"125","author":"Shen","year":"2010","journal-title":"Pediatrics"},{"key":"R52-43-20210317","first-page":"1782","article-title":"Genetic predisposition in degenerative lumbar scoliosis due to the copy number variation. Spine (Phila Pa 1976).","volume":"36","author":"Shin","year":"2011","journal-title":""},{"key":"R57-43-20210317","doi-asserted-by":"crossref","first-page":"602","DOI":"10.1038\/ejhg.2013.203","article-title":"Copy number variants in patients with short stature.","volume":"22","author":"van Duyvenvoorde","year":"2014","journal-title":"Eur J Hum Genet"},{"key":"R61-43-20210317","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1302\/0301-620X.50B1.24","article-title":"Familial (idiopathic) scoliosis: a family survey.","volume":"50","author":"Wynne-Davies","year":"1968","journal-title":"J Bone Joint Surg Br"}],"container-title":["Clinical Orthopaedics & Related Research"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/00003086-201410000-00043","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,3,17]],"date-time":"2021-03-17T11:19:55Z","timestamp":1615979995000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00003086-201410000-00043"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,10]]},"references-count":12,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2014]]}},"URL":"https:\/\/doi.org\/10.1007\/s11999-014-3766-8","relation":{},"ISSN":["0009-921X"],"issn-type":[{"value":"0009-921X","type":"print"}],"subject":[],"published":{"date-parts":[[2014,10]]}}}