{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:07:28Z","timestamp":1761718048631},"reference-count":12,"publisher":"Springer Science and Business Media LLC","issue":"6","license":[{"start":{"date-parts":[[2007,11,28]],"date-time":"2007-11-28T00:00:00Z","timestamp":1196208000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatr Cardiol"],"published-print":{"date-parts":[[2008,11]]},"DOI":"10.1007\/s00246-007-9150-7","type":"journal-article","created":{"date-parts":[[2007,11,27]],"date-time":"2007-11-27T10:41:01Z","timestamp":1196160061000},"page":"1104-1106","source":"Crossref","is-referenced-by-count":14,"title":["D-Transposition of the Great Arteries in a Case of Microduplication 22q11.2"],"prefix":"10.1007","volume":"29","author":[{"given":"Gitta","family":"Laitenberger","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Birgit","family":"Donner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Juergen","family":"Gebauer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Thomas","family":"Hoehn","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2007,11,28]]},"reference":[{"key":"9150_CR1","first-page":"269","volume":"135","author":"CH Attenhofer Jost","year":"2005","unstructured":"Attenhofer Jost CH, Connolly HM, Edwards WD, Hayes D, Warnes CA, Danielson GK (2005) Ebstein\u2019s anomaly\u2014review of a multifaceted congenital cardiac condition. Swiss Med Wkly 135:269\u2013281","journal-title":"Swiss Med Wkly"},{"key":"9150_CR2","doi-asserted-by":"crossref","first-page":"9073","DOI":"10.1016\/S0022-3476(65)82145-X","volume":"67","author":"A DiGeorge","year":"1965","unstructured":"DiGeorge A (1965) A new concept of the cellular basis of immunity. J Pediatr 67:9073","journal-title":"J Pediatr"},{"key":"9150_CR3","doi-asserted-by":"crossref","first-page":"1027","DOI":"10.1086\/378818","volume":"73","author":"RE Ensenauer","year":"2003","unstructured":"Ensenauer RE, Adeyinka A, Flynn HC, Michels VV, Lindor NM, Dawson DB, Thorland EC, Lorentz CP, Goldstein JL, Mc Donald MT, Smith WE, Simon-Fayard E, Alexander AA, Kulharya AS, Ketterling RP, Clark RD, Jalal SM (2003) Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic and molecular analysis of thirteen patients. Am J Hum Genet 73:1027\u20131040","journal-title":"Am J Hum Genet"},{"key":"9150_CR4","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1016\/S0022-3476(89)80605-5","volume":"114","author":"C Ferencz","year":"1989","unstructured":"Ferencz C, Neill CA, Boughman JA, Rubin JD, Brenner JI, Perry LW (1989) Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study. J Pediatr 114:79\u201386","journal-title":"J Pediatr"},{"key":"9150_CR5","doi-asserted-by":"crossref","first-page":"400","DOI":"10.1111\/j.0009-9163.2004.0212.x","volume":"65","author":"SJ Hassed","year":"2004","unstructured":"Hassed SJ, Hopcus-Niccum D, Zhang L, Li S, Mulvihill JJ (2004) A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clin Genet 65:400\u2013404","journal-title":"Clin Genet"},{"key":"9150_CR6","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1016\/S0002-9149(99)80541-4","volume":"75","author":"S Melchionda","year":"1995","unstructured":"Melchionda S, Digilio MC, Mingarelli R, Novelli G, Scambler P, Marino B, Dallapiccola B (1995) Transposition of the great arteries associated with deletion of chromosome 22q11.2. Am J Cardiol 75:95\u201398","journal-title":"Am J Cardiol"},{"key":"9150_CR7","doi-asserted-by":"crossref","first-page":"798","DOI":"10.1136\/jmg.34.10.798","volume":"34","author":"AK Ryan","year":"1997","unstructured":"Ryan AK, Goodship JA, Wilson DI, Philip N, Levy A, Seidel H, Schuffenhauer S, Oechsler H, Belohradsky B, Prieur M, Aurias A, Raymond FL, Clayton-Smith J, Hatchwell E, McKeown C, Beemer FA, Dallapiccola B, Novelli G, Hurst JA, Ignatius J, Green AJ, Winter RM, Brueton L, Brondum-Nielsen K, Stewart F, Van Essen T, Patton M, Paterson J, Scambler PJ (1997) Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: an european collaborative study. J Med Genet 34:798\u2013804","journal-title":"J Med Genet"},{"key":"9150_CR8","first-page":"56","volume":"15","author":"RJ Shprintzen","year":"1978","unstructured":"Shprintzen RJ, Goldberg RB, Lewin ML, et al. (1978) A new syndrome involving cleft palate, cardiac anomalies, typical facies and learning disabilities: velo-cardio-facial syndrome. Cleft Palate J 15:56\u201362","journal-title":"Cleft Palate J"},{"key":"9150_CR9","doi-asserted-by":"crossref","first-page":"725","DOI":"10.1097\/01.mop.0000184465.73833.0b","volume":"17","author":"RJ Shprintzen","year":"2005","unstructured":"Shprintzen RJ, Higgins AM, Antshel K, Fremot W, Roizen N, Kates W (2005) Velo-cardio-facial syndrome. Curr Opin Pediatr 17:725\u2013730","journal-title":"Curr Opin Pediatr"},{"key":"9150_CR10","doi-asserted-by":"crossref","first-page":"229","DOI":"10.1017\/S1047951105000466","volume":"15","author":"R Sparkes","year":"2005","unstructured":"Sparkes R, Chernos J, Dicke F (2005) Duplication of the 22q11.2 region associated with congenital cardiac disease. Cardiol Young 15:229\u2013231","journal-title":"Cardiol Young"},{"key":"9150_CR11","first-page":"79","volume":"10","author":"A Swillen","year":"1999","unstructured":"Swillen A, Devriendt K, Legius E, Prinzie P, Vogels A, Ghesquiere P, Fryns JP (1999) The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genet Couns 10:79\u201388","journal-title":"Genet Couns"},{"key":"9150_CR12","doi-asserted-by":"crossref","first-page":"865","DOI":"10.1086\/429841","volume":"76","author":"TM Yobb","year":"2005","unstructured":"Yobb TM, Somerville MJ, Willatt L, Firth HV, Harrison K, MacKenzie J, Gallo N, Morrow BE, Shaffer LG, Babcock M, Chernos J, Bernier F, Sprysak K, Christiansen J, Haase S, Elyas B, Lilley M, Bamforth S, Mc Dermid HE (2005) Microduplication and triplication of 22q11.2: a highly variable syndrome. Am J Hum Genet. 76:865\u2013876","journal-title":"Am J Hum Genet."}],"container-title":["Pediatric Cardiology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00246-007-9150-7.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00246-007-9150-7\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00246-007-9150-7","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,24]],"date-time":"2019-05-24T10:11:51Z","timestamp":1558692711000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00246-007-9150-7"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,11,28]]},"references-count":12,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2008,11]]}},"alternative-id":["9150"],"URL":"https:\/\/doi.org\/10.1007\/s00246-007-9150-7","relation":{},"ISSN":["0172-0643","1432-1971"],"issn-type":[{"value":"0172-0643","type":"print"},{"value":"1432-1971","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,11,28]]}}}