{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,11]],"date-time":"2023-10-11T05:19:38Z","timestamp":1697001578443},"reference-count":4,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2003,6,12]],"date-time":"2003-06-12T00:00:00Z","timestamp":1055376000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2003,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report on a pair of dizygotic twins born to consanguineous parents, showing an extreme delay in skeletal maturation (roughly corresponding to the time of birth at the age of 4 10\/12 years), mild metaphyseal irregularities, and normal to large stature (+\u20091 to +\u20092 SD) with normal growth pattern, long fingers, generalized small joint hyperlaxity with flat feet, genua valga, and low normal intellectual development. This disorder was not associated with abnormal endocrine function or abnormal Ca\/P metabolism. This epiphyseal disorder is compatible with autosomal recessive inheritance.\u00a9 2003 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.20046","type":"journal-article","created":{"date-parts":[[2003,7,23]],"date-time":"2003-07-23T10:12:06Z","timestamp":1058955126000},"page":"553-556","source":"Crossref","is-referenced-by-count":1,"title":["Severely delayed epiphyseal ossification dysplasia with normal stature"],"prefix":"10.1002","volume":"120A","author":[{"given":"Clarisse","family":"Baumann","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Catherine","family":"Garel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lucille","family":"Vuillemain","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Max","family":"Hassan","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alain","family":"Verloes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2003,6,12]]},"reference":[{"key":"e_1_2_5_2_1","volume-title":"Syndromes dysmorphiques et maladies constitutionnelles du squelette","author":"Canepa G","year":"1999"},{"key":"e_1_2_5_3_1","volume-title":"Radiological electronic atlas of malformation syndromes (REAMS)","author":"Hall C","year":"2000"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1007\/978-1-4471-0295-3"},{"key":"e_1_2_5_5_1","first-page":"67","volume-title":"The hand in radiologic diagnosis","author":"Poznanski AK","year":"1984"}],"container-title":["American Journal of Medical Genetics Part A"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.a.20046","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.a.20046","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,10]],"date-time":"2023-10-10T14:14:09Z","timestamp":1696947249000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.a.20046"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2003,6,12]]},"references-count":4,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2003,8]]}},"alternative-id":["10.1002\/ajmg.a.20046"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.a.20046","archive":["Portico"],"relation":{},"ISSN":["1552-4825","1552-4833"],"issn-type":[{"value":"1552-4825","type":"print"},{"value":"1552-4833","type":"electronic"}],"subject":[],"published":{"date-parts":[[2003,6,12]]}}}