{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,12,29]],"date-time":"2023-12-29T21:20:16Z","timestamp":1703884816403},"reference-count":10,"publisher":"Springer Science and Business Media LLC","issue":"1-2","license":[{"start":{"date-parts":[[1986,4,1]],"date-time":"1986-04-01T00:00:00Z","timestamp":512697600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Pediatr"],"published-print":{"date-parts":[[1986,4]]},"DOI":"10.1007\/bf00441869","type":"journal-article","created":{"date-parts":[[2004,11,12]],"date-time":"2004-11-12T03:26:24Z","timestamp":1100229984000},"page":"116-118","source":"Crossref","is-referenced-by-count":7,"title":["Severe pulmonary arterial stenoses in Conradi-H\ufffdnermann disease"],"prefix":"10.1007","volume":"145","author":[{"given":"E.","family":"Trowitzsch","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Richter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"W.","family":"Eisenberg","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H. C.","family":"Kallfelz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"63","DOI":"10.1016\/S0022-3476(75)80706-2","volume":"86","author":"D Allagille","year":"1975","unstructured":"Allagille D, Odievre M, Gautier M, Dommergues JP (1975) Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr 86:63?71","journal-title":"J Pediatr"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1016\/0002-9149(64)90154-7","volume":"13","author":"AJ Beuren","year":"1964","unstructured":"Beuren AJ, Schulze C, Eberle P, Harmjanz D, Apitz J (1964) The syndrome of supravalvular aortic stenosis, peripheral pulmonary stenosis, mental retardation, and similar facial appearance. Am J Cardiol 13:471?483","journal-title":"Am J Cardiol"},{"key":"CR3","first-page":"599","volume":"90","author":"BB Gay","year":"1963","unstructured":"Gay BB, Franch RH, Shuford WH, Rogers VJ (1963) Roentgenologic features of simple and multiple coarctations of the pulmonary artery and branches. Am J Roentgenol 90:599?613","journal-title":"Am J Roentgenol"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1007\/BF00289453","volume":"53","author":"R Happle","year":"1979","unstructured":"Happle R (1979) X-linked dominant chondrodysplasia punctata. Review of literature and report of a case. Hum Genet 53:65?73","journal-title":"Hum Genet"},{"key":"CR5","volume-title":"Heart disease in infancy and childhood","author":"JD Keith","year":"1978","unstructured":"Keith JD, Rowe RD, Vlad P (1978) Heart disease in infancy and childhood, 3rd edn. MacMillan, New York","edition":"3rd edn."},{"key":"CR6","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1001\/archpedi.1968.02100020377005","volume":"116","author":"JA Noonan","year":"1968","unstructured":"Noonan JA (1968) Hypertelorism with Turner phenotype: A new syndrome with associated congenital heart disease. Am J Dis Child 116:373?380","journal-title":"Am J Dis Child"},{"key":"CR7","first-page":"61","volume":"5","author":"RD Rowe","year":"1973","unstructured":"Rowe RD (1973) Cardiovascular disease in the rubella syndrome. Cardiovasc Clin 5:61?80","journal-title":"Cardiovasc Clin"},{"key":"CR8","unstructured":"Salmon MA (1978) In: Developmental defects and syndromes, edited by HM+M publishers, pp 268?270"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"911","DOI":"10.1016\/S0022-3476(80)80419-7","volume":"97","author":"MC Silengo","year":"1980","unstructured":"Silengo MC, Luzzatti L, Silverman FN (1980) Clinical and genetic aspects of Conradi-H\ufffdnermann disease. J Pediatr 97:911?917","journal-title":"J Pediatr"},{"key":"CR10","first-page":"190","volume":"11","author":"JW Spranger","year":"1971","unstructured":"Spranger JW, Opitz JM, Bidder U (1971) Heterogeneity of chondrodysplasia punctata. Humgenetik 11:190?212","journal-title":"Humgenetik"}],"container-title":["European Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00441869.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00441869\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00441869","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,4]],"date-time":"2019-04-04T00:38:16Z","timestamp":1554338296000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00441869"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1986,4]]},"references-count":10,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[1986,4]]}},"alternative-id":["BF00441869"],"URL":"https:\/\/doi.org\/10.1007\/bf00441869","relation":{},"ISSN":["0340-6199","1432-1076"],"issn-type":[{"value":"0340-6199","type":"print"},{"value":"1432-1076","type":"electronic"}],"subject":[],"published":{"date-parts":[[1986,4]]}}}