{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,21]],"date-time":"2025-11-21T12:09:13Z","timestamp":1763726953474},"reference-count":11,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[2015,10,28]],"date-time":"2015-10-28T00:00:00Z","timestamp":1445990400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["J Med Case Reports"],"published-print":{"date-parts":[[2015,12]]},"DOI":"10.1186\/s13256-015-0724-3","type":"journal-article","created":{"date-parts":[[2015,10,28]],"date-time":"2015-10-28T10:11:15Z","timestamp":1446027075000},"update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":3,"title":["A rare association - amelogenesis imperfecta, platispondyly and bicytopenia: a case report"],"prefix":"10.1186","volume":"9","author":[{"given":"Samir","family":"Laouina","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Siham","family":"Chafai El Alaoui","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rachida","family":"Amezian","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abderrahmane","family":"Al Bouzidi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abdelaziz.","family":"Sefiani","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mustapha","family":"El Alloussi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2015,10,28]]},"reference":[{"key":"724_CR1","doi-asserted-by":"publisher","first-page":"e579","DOI":"10.4317\/medoral.14.e579","volume":"14","author":"Z Kirzioglu","year":"2009","unstructured":"Kirzioglu Z, Ulu KG, Sezer MT, Yuksel S. The relationship of amelogenesis imperfecta and nephrocalcinosis syndrome. Med Oral Patol Oral Cir Bucal. 2009;14:e579\u2013582.","journal-title":"Med Oral Patol Oral Cir Bucal."},{"key":"724_CR2","doi-asserted-by":"publisher","first-page":"547","DOI":"10.1111\/j.1600-0714.1988.tb01332.x","volume":"17","author":"CJ Witkop Jr","year":"1988","unstructured":"Witkop Jr CJ. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol. 1988;17:547\u201353.","journal-title":"J Oral Pathol."},{"key":"724_CR3","doi-asserted-by":"publisher","first-page":"17","DOI":"10.1186\/1750-1172-2-17","volume":"2","author":"PJ Crawford","year":"2007","unstructured":"Crawford PJ, Aldred M, Bloch-Zupan A. Amelogenesis imperfecta. Orphanet J Rare Dis. 2007;2:17.","journal-title":"Orphanet J Rare Dis."},{"key":"724_CR4","doi-asserted-by":"publisher","first-page":"19","DOI":"10.1034\/j.1601-0825.2003.00843.x","volume":"9","author":"MJ Aldred","year":"2003","unstructured":"Aldred MJ, Savarirayan R, Crawford PJ. Amelogenesis imperfecta: a classification and catalogue for the 21st century. Oral Dis. 2003;9:19\u201323.","journal-title":"Oral Dis."},{"key":"724_CR5","doi-asserted-by":"publisher","first-page":"272","DOI":"10.1002\/ajmg.a.20204","volume":"120a","author":"M Mukamel","year":"2003","unstructured":"Mukamel M, Karmazyn B, de Vries L, Horev G, Shohat M. Brachyolmia and spinal stenosis. Am J Med Genet A. 2003;120a:272\u20135.","journal-title":"Am J Med Genet A"},{"key":"724_CR6","doi-asserted-by":"publisher","first-page":"2","DOI":"10.1111\/j.1399-0004.1996.tb04315.x","volume":"49","author":"A Verloes","year":"1996","unstructured":"Verloes A, Jamblin P, Koulischer L, Bourguignon JP. A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly. Clin Genet. 1996;49:2\u20135.","journal-title":"Clin Genet."},{"key":"724_CR7","doi-asserted-by":"publisher","first-page":"532","DOI":"10.1002\/ajmg.a.32661","volume":"149a","author":"DR Bertola","year":"2009","unstructured":"Bertola DR, Antequera R, Rodovalho MJ, Honjo RS, Albano LM, Furquim IM, et al. Brachyolmia with amelogenesis imperfecta: further evidence of a distinct entity. Am J Med Genet A. 2009;149a:532\u20134.","journal-title":"Am J Med Genet A"},{"key":"724_CR8","doi-asserted-by":"publisher","first-page":"3038","DOI":"10.1093\/hmg\/ddv053","volume":"24","author":"M Huckert","year":"2015","unstructured":"Huckert M, Stoetzel C, Morkmued S, Laugel-Haushalter V, Geoffroy V, Muller J, et al. Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta. Hum Mol Genet. 2015;24:3038\u201349.","journal-title":"Hum Mol Genet."},{"key":"724_CR9","doi-asserted-by":"publisher","first-page":"659","DOI":"10.1515\/JPEM.2002.15.5.659","volume":"15","author":"B Dundar","year":"2002","unstructured":"Dundar B, Ercal D, Bober E, Berk T, Buyukgebiz A. Amelogenesis imperfecta with growth hormone deficiency in a 12 year-old boy. J Pediatr Endocrinol Metab. 2002;15:659\u201362.","journal-title":"J Pediatr Endocrinol Metab."},{"key":"724_CR10","doi-asserted-by":"publisher","first-page":"64","DOI":"10.3389\/fped.2015.00064","volume":"3","author":"M Erlacher","year":"2015","unstructured":"Erlacher M, Strahm B. Missing cells: pathophysiology, diagnosis, and management of (pan)cytopenia in childhood. Front Pediatr. 2015;3:64.","journal-title":"Front Pediatr."},{"key":"724_CR11","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1542\/peds.67.1.119","volume":"67","author":"J Cervenka","year":"1981","unstructured":"Cervenka J, Arthur D, Yasis C. Mitomycin C test for diagnostic differentiation of idiopathic aplastic anemia and Fanconi anemia. Pediatrics. 1981;67:119\u201327.","journal-title":"Pediatrics."}],"container-title":["Journal of Medical Case Reports"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/s13256-015-0724-3.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1186\/s13256-015-0724-3\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1186\/s13256-015-0724-3.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,5,24]],"date-time":"2022-05-24T17:04:13Z","timestamp":1653411853000},"score":1,"resource":{"primary":{"URL":"http:\/\/jmedicalcasereports.biomedcentral.com\/articles\/10.1186\/s13256-015-0724-3"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,10,28]]},"references-count":11,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2015,12]]}},"alternative-id":["724"],"URL":"https:\/\/doi.org\/10.1186\/s13256-015-0724-3","relation":{},"ISSN":["1752-1947"],"issn-type":[{"value":"1752-1947","type":"electronic"}],"subject":[],"published":{"date-parts":[[2015,10,28]]},"article-number":"245"}}