{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,19]],"date-time":"2026-02-19T19:39:29Z","timestamp":1771529969985,"version":"3.50.1"},"reference-count":18,"publisher":"Springer Science and Business Media LLC","issue":"10","license":[{"start":{"date-parts":[[2008,8,12]],"date-time":"2008-08-12T00:00:00Z","timestamp":1218499200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatr Surg Int"],"published-print":{"date-parts":[[2008,10]]},"DOI":"10.1007\/s00383-008-2222-9","type":"journal-article","created":{"date-parts":[[2008,8,11]],"date-time":"2008-08-11T16:12:48Z","timestamp":1218471168000},"page":"1153-1156","source":"Crossref","is-referenced-by-count":12,"title":["Esophageal atresia and tracheo-esophageal fistula associated with coarctation of the aorta, CHARGE association, and DiGeorge syndrome: a case report and literature review"],"prefix":"10.1007","volume":"24","author":[{"given":"Kyeong Deok","family":"Lee","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tadaharu","family":"Okazaki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshifumi","family":"Kato","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Geoffrey J.","family":"Lane","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Atsuyuki","family":"Yamataka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2008,8,12]]},"reference":[{"key":"2222_CR1","doi-asserted-by":"crossref","first-page":"789","DOI":"10.1136\/jmg.35.9.789-a","volume":"35","author":"K Devriendt","year":"1998","unstructured":"Devriendt K, Fryna JP, Mortier G, van Thienen MN, Keymolen K (1998) The annual incidence of DiGeorge\/velocardiofacial syndrome. J Med Genet 35:789\u2013790","journal-title":"J Med Genet"},{"key":"2222_CR2","doi-asserted-by":"crossref","first-page":"4539","DOI":"10.1182\/blood-2006-10-048652","volume":"109","author":"ML Markert","year":"2007","unstructured":"Markert ML, Devlin BH, Alexieff MJ, Li J, McCarthy EA, Gupton SE (2007) Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants. Blood 109:4539\u20134547","journal-title":"Blood"},{"key":"2222_CR3","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1016\/S0022-3476(81)80454-4","volume":"99","author":"RA Pagon","year":"1981","unstructured":"Pagon RA, Graham JM Jr, Zonana J, Yong SL (1981) Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association. J Pediatr 99:223\u2013227","journal-title":"J Pediatr"},{"key":"2222_CR4","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1038\/sj.ejhg.5201778","volume":"15","author":"D Sanlaville","year":"2007","unstructured":"Sanlaville D, Verloes A (2007) CHARGE syndrome: an update. Eur J Hum Genet 15:389\u2013399","journal-title":"Eur J Hum Genet"},{"key":"2222_CR5","doi-asserted-by":"crossref","first-page":"986","DOI":"10.1136\/jmg.34.12.986","volume":"34","author":"P Lonlay-Debeney de","year":"1997","unstructured":"de Lonlay-Debeney P, Cormier-Daire V, Amiel J, Abadie V, Odent S, Paupe A (1997) Features of DiGeorge syndrome and CHARGE association in five patients. J Med Genet 34:986\u2013989","journal-title":"J Med Genet"},{"key":"2222_CR6","doi-asserted-by":"crossref","first-page":"183","DOI":"10.1016\/S0387-7604(98)00013-8","volume":"20","author":"LA Squires","year":"1998","unstructured":"Squires LA, Dieffenbach AZ, Betz BW (1998) Three malformation complexes related to neural crest development. Brain Dev 20:183\u2013185","journal-title":"Brain Dev"},{"key":"2222_CR7","doi-asserted-by":"crossref","first-page":"441","DOI":"10.1111\/j.1399-3046.2007.00702.x","volume":"11","author":"A Janda","year":"2007","unstructured":"Janda A, Sedlacek P, Mejstrikova E, Zdrahalova K, Hrusak O, Kalina T, Sieglova Z, Zizkova H, Formankova R, Keslova P, Hubacek P, Sediva A, Bartunkova J, Dlask K, Stary J (2007) Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge\/CHARGE syndrome. Pediatr Transplant 11:441\u2013447","journal-title":"Pediatr Transplant"},{"key":"2222_CR8","doi-asserted-by":"crossref","first-page":"364","DOI":"10.1002\/(SICI)1099-0496(199711)24:5<364::AID-PPUL9>3.0.CO;2-I","volume":"24","author":"ML Markert","year":"1997","unstructured":"Markert ML, Majure M, Harville TO, Hulka G, Oldham K (1997) Severe laryngomalacia and bronchomalacia in DiGeorge syndrome and CHARGE association. Pediatric Pulmonol 24:364\u2013369","journal-title":"Pediatric Pulmonol"},{"key":"2222_CR9","doi-asserted-by":"crossref","first-page":"927","DOI":"10.1038\/sj.bmt.1701475","volume":"22","author":"T Matsumo","year":"1998","unstructured":"Matsumo T, Amamoto N, Kondoh T (1998) Complete DiGeorge syndrome treated by bone marrow transplantation. Bone Marrow Transplant 22:927\u2013930","journal-title":"Bone Marrow Transplant"},{"key":"2222_CR10","doi-asserted-by":"crossref","first-page":"1180","DOI":"10.1056\/NEJM199910143411603","volume":"341","author":"ML Markert","year":"1999","unstructured":"Markert ML, Boeck A, Hale LP (1999) Transplantation of thymus tissue in complete DiGeorge syndrome. N Engl J Med 341:1180\u20131189","journal-title":"N Engl J Med"},{"key":"2222_CR11","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1136\/adc.65.2.217","volume":"65","author":"KD Blake","year":"1990","unstructured":"Blake KD, Rusell-Eggitt IM, Morgan DW (1990) Who\u2019s in CHARGE? Multidisciplinary management of patients with CHARGE association. Arch Dis Child 65:217\u2013223","journal-title":"Arch Dis Child"},{"key":"2222_CR12","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1016\/0022-3468(92)90445-D","volume":"27","author":"M Kutiyanawala","year":"1992","unstructured":"Kutiyanawala M, Wyse H, Brereton R (1992) CHARGE and esophageal atresia. J Pediatr Surg 27:558\u2013560","journal-title":"J Pediatr Surg"},{"key":"2222_CR13","first-page":"560","volume-title":"The developing human. Clinically oriented embryology","author":"KL Moore","year":"2003","unstructured":"Moore KL, Persaud TVN (2003) The developing human. Clinically oriented embryology, 7th edn. Saunders, Philadelphia, p 560","edition":"7"},{"key":"2222_CR14","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1053\/jpsu.2003.50037","volume":"38","author":"AK Williams","year":"2003","unstructured":"Williams AK, Quan QB, Beasley SW (2003) Three-dimensional imaging clarifies the process of tracheoesophageal separation in the rat. J Pediatr Surg 38:173\u2013177","journal-title":"J Pediatr Surg"},{"key":"2222_CR15","doi-asserted-by":"crossref","first-page":"915","DOI":"10.1016\/j.jpedsurg.2007.01.022","volume":"42","author":"LG Stephen","year":"2007","unstructured":"Stephen LG (2007) The neural crest in pediatric surgery. J Pediatr Surg 42:915\u2013926","journal-title":"J Pediatr Surg"},{"key":"2222_CR16","doi-asserted-by":"crossref","first-page":"955","DOI":"10.1038\/ng1407","volume":"36","author":"LE Vissers","year":"2004","unstructured":"Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, Janssen IM, van der Vliet WA, Huys EH, de Jong PJ, Hamel BC, Schoenmakers EF, Brunner HG, Veltman JA, van Kessel AG (2004) Mutations in anew member of the chromodomain gene family cause CHARGE syndrome. Nat Genet 36:955\u2013957","journal-title":"Nat Genet"},{"issue":"4","key":"2222_CR17","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1136\/jmg.2005.036061","volume":"43","author":"M Jongmans","year":"2006","unstructured":"Jongmans M, Admiraal R, van der Donk K, Vissers L, Baas A, Kapusta L, van Hagen JM, Donnai D, de Ravel T, Veltman J, Geurts van Kessel A, de Vries B, Brunner H, Hoefsloot L, van Ravenswaaij C (2006) CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. Med Genet 43(4):306\u2013314","journal-title":"Med Genet"},{"issue":"3","key":"2222_CR18","doi-asserted-by":"crossref","first-page":"510","DOI":"10.1086\/511993","volume":"80","author":"Z Christiane","year":"2007","unstructured":"Christiane Z, Heinrich S, Inci A, ECl Christine, Anita R (2007) Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions. Am J Hum Genet 80(3):510\u2013517","journal-title":"Am J Hum Genet"}],"container-title":["Pediatric Surgery International"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00383-008-2222-9.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00383-008-2222-9\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00383-008-2222-9","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,28]],"date-time":"2019-05-28T15:52:11Z","timestamp":1559058731000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00383-008-2222-9"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,8,12]]},"references-count":18,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2008,10]]}},"alternative-id":["2222"],"URL":"https:\/\/doi.org\/10.1007\/s00383-008-2222-9","relation":{},"ISSN":["0179-0358","1437-9813"],"issn-type":[{"value":"0179-0358","type":"print"},{"value":"1437-9813","type":"electronic"}],"subject":[],"published":{"date-parts":[[2008,8,12]]}}}