{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,29]],"date-time":"2025-09-29T20:31:51Z","timestamp":1759177911496},"reference-count":16,"publisher":"Springer Science and Business Media LLC","issue":"6","license":[{"start":{"date-parts":[[2009,5,27]],"date-time":"2009-05-27T00:00:00Z","timestamp":1243382400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[2009,5,27]],"date-time":"2009-05-27T00:00:00Z","timestamp":1243382400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["J Perinatol"],"published-print":{"date-parts":[[2009,6]]},"DOI":"10.1038\/jp.2008.208","type":"journal-article","created":{"date-parts":[[2009,5,28]],"date-time":"2009-05-28T11:21:20Z","timestamp":1243509680000},"page":"455-457","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Beckwith\u2013Wiedemann syndrome associated with congenital hypothyroidism in a preterm neonate: a case report and literature review"],"prefix":"10.1038","volume":"29","author":[{"given":"G I","family":"Ramadan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N L","family":"Kennea","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2009,5,27]]},"reference":[{"key":"BFjp2008208_CR1","doi-asserted-by":"publisher","first-page":"873","DOI":"10.1016\/S0022-3476(83)80014-6","volume":"102","author":"M Waziri","year":"1983","unstructured":"Waziri M, Patil SR, Hanson JW, Bartley JA . Abnormality of chromosome 11 in patients with features of Beckwith\u2013Wiedemann syndrome. J Pediatr 1983; 102: 873\u2013876.","journal-title":"J Pediatr"},{"key":"BFjp2008208_CR2","doi-asserted-by":"publisher","first-page":"41","DOI":"10.1002\/ajmg.1320240107","volume":"24","author":"N Nikawa","year":"1986","unstructured":"Nikawa N, Ishikiriyama S, Takahashi S . The Wiedemann\u2013Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity. Am J Med Genet 1986; 24: 41\u201355.","journal-title":"Am J Med Genet"},{"key":"BFjp2008208_CR3","doi-asserted-by":"publisher","first-page":"560","DOI":"10.1136\/jmg.31.7.560","volume":"31","author":"M Elliott","year":"1994","unstructured":"Elliott M, Maher ER . Beckwith\u2013Wiedemann syndrome. J Med Genet 1994; 31: 560\u2013564.","journal-title":"J Med Genet"},{"key":"BFjp2008208_CR4","doi-asserted-by":"publisher","first-page":"143","DOI":"10.1007\/BF00282078","volume":"74","author":"MJ Pettenati","year":"1986","unstructured":"Pettenati MJ, Haines JL, Higgins RR, Wappner RS, Palmer CG, Weaver DD . Wiedemann\u2013Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Hum Genet 1986; 74: 143\u2013154.","journal-title":"Hum Genet"},{"issue":"Suppl","key":"BFjp2008208_CR5","first-page":"A50","volume":"7","author":"ME Carlin","year":"1990","unstructured":"Carlin ME, Escobar LF, Ward RE, Wielgus TY . A reassessment of Beckwith\u2013Wiedemann syndrome (BWS) (abstract). Am J Hum Genet 1990; 7 (Suppl): A50.","journal-title":"Am J Hum Genet"},{"key":"BFjp2008208_CR6","doi-asserted-by":"publisher","first-page":"434","DOI":"10.1002\/ajmg.1320360412","volume":"36","author":"D Chitayat","year":"1990","unstructured":"Chitayat D, Rothchild A, Ling E, Friedman JM, Couch RM, Yong SL et al. Apparent postnatal onset of some manifestation of the Wiedemann\u2013Beckwith syndrome. Am J Med Genet 1990; 36: 434\u2013439.","journal-title":"Am J Med Genet"},{"key":"BFjp2008208_CR7","doi-asserted-by":"publisher","first-page":"129","DOI":"10.1007\/BF00496807","volume":"141","author":"HR Weidemann","year":"1983","unstructured":"Weidemann HR . Tumours and hemihypertrophy associated with Wiedemann\u2013Beckwith syndrome. Eur J Pediatr 1983; 141: 129.","journal-title":"Eur J Pediatr"},{"key":"BFjp2008208_CR8","doi-asserted-by":"publisher","first-page":"233","DOI":"10.1007\/BF00442150","volume":"143","author":"R Mart\u00ednez y Mart\u00ednez","year":"1985","unstructured":"Mart\u00ednez y Mart\u00ednez R, Ocampo-Campos R, P\u00e9rez-Arroyo R, Corona-Rivera E, Cant\u00fa JM . The Wiedemann\u2013Beckwith syndrome in four sibs including one with associated congenital hypothyroidism. Eur J Pediatr 1985; 143: 233\u2013235.","journal-title":"Eur J Pediatr"},{"key":"BFjp2008208_CR9","doi-asserted-by":"publisher","first-page":"20","DOI":"10.1111\/j.1399-0004.1989.tb02901.x","volume":"35","author":"WG Sippell","year":"1989","unstructured":"Sippell WG, Partsch CJ, Wiedemann HR . Growth, bone maturation and pubertal development in children with the EMG-syndrome. Clin Genet 1989; 35: 20\u201328.","journal-title":"Clin Genet"},{"key":"BFjp2008208_CR10","first-page":"132","volume":"89","author":"CH Chien","year":"1990","unstructured":"Chien CH, Lee JS, Tsai WY, Wang TR . Wiedemann\u2013Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins. J Formos Med Assoc 1990; 89: 132\u2013136.","journal-title":"J Formos Med Assoc"},{"key":"BFjp2008208_CR11","first-page":"10","volume":"28","author":"M Vidaihet","year":"1971","unstructured":"Vidaihet M, Rauber G, Grigon G, Ratajczak F, Neimann N, Pierson M . Syndrome de Beckwith\u2013Wiedemann. \u00c9tude de quarte observations, donte une avec n\u00e9phroblastoma. Arch Franc Ped 1971; 28: 10\u201311.","journal-title":"Arch Franc Ped"},{"key":"BFjp2008208_CR12","first-page":"63","volume":"118","author":"SL Kaufmann","year":"1973","unstructured":"Kaufmann SL, Frederickson R . Thyroxin-binding globulin deficiency in a patient with Beckwith syndrome. Calif Med 1973; 118: 63\u201366.","journal-title":"Calif Med"},{"key":"BFjp2008208_CR13","doi-asserted-by":"publisher","first-page":"752","DOI":"10.1016\/S0022-3476(79)80730-1","volume":"95","author":"AK Leung","year":"1979","unstructured":"Leung AK, McArthur RG, Ross SA, McMillan DD, Sauve RS . Thyroxin binding globulin deficiency in Beckwith syndrome. J Pediatr 1979; 95: 752\u2013754.","journal-title":"J Pediatr"},{"key":"BFjp2008208_CR14","doi-asserted-by":"publisher","first-page":"871","DOI":"10.1089\/105072501316973136","volume":"11","author":"DA Paul","year":"2001","unstructured":"Paul DA, Leef KH, Voss B, Stefano JL, Bartoshesky L . Thyroxine and illness severity in very low-birth-weight infants. Thyroid 2001; 11: 871\u2013875.","journal-title":"Thyroid"},{"key":"BFjp2008208_CR15","doi-asserted-by":"publisher","first-page":"269","DOI":"10.1111\/j.1399-0004.1989.tb03202.x","volume":"36","author":"AKC Leung","year":"1989","unstructured":"Leung AKC, McArthur RG . EMG-syndrome and hypothyroidism. Clin Genet 1989; 36: 269.","journal-title":"Clin Genet"},{"key":"BFjp2008208_CR16","doi-asserted-by":"publisher","first-page":"503","DOI":"10.1093\/hmg\/ddi047","volume":"14","author":"F Cerrato","year":"2005","unstructured":"Cerrato F, Sparago A, Di Matteo I, Zou X, Dean W, Sasaki H et al. The two-domain hypothesis in Beckwith\u2013Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster. Hum Mol Genet 2005; 14: 503\u2013511.","journal-title":"Hum Mol Genet"}],"container-title":["Journal of Perinatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.nature.com\/articles\/jp2008208.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/jp2008208","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/www.nature.com\/articles\/jp2008208.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,3,18]],"date-time":"2022-03-18T12:17:14Z","timestamp":1647605834000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.nature.com\/articles\/jp2008208"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,5,27]]},"references-count":16,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2009,6]]}},"alternative-id":["BFjp2008208"],"URL":"https:\/\/doi.org\/10.1038\/jp.2008.208","relation":{},"ISSN":["0743-8346","1476-5543"],"issn-type":[{"value":"0743-8346","type":"print"},{"value":"1476-5543","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,5,27]]},"assertion":[{"value":"13 July 2008","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"5 October 2008","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"28 October 2008","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"27 May 2009","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}}]}}