{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,2]],"date-time":"2022-04-02T19:28:05Z","timestamp":1648927685168},"reference-count":15,"publisher":"Springer Science and Business Media LLC","issue":"12","license":[{"start":{"date-parts":[[2000,12,1]],"date-time":"2000-12-01T00:00:00Z","timestamp":975628800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Indian J Pediatr"],"published-print":{"date-parts":[[2000,12]]},"DOI":"10.1007\/bf02723962","type":"journal-article","created":{"date-parts":[[2007,10,16]],"date-time":"2007-10-16T02:02:47Z","timestamp":1192500167000},"page":"935-937","source":"Crossref","is-referenced-by-count":2,"title":["Hypospadias-hypertelorism syndrome"],"prefix":"10.1007","volume":"67","author":[{"given":"Jatinder S.","family":"Goraya","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A. S.","family":"Bawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sahul","family":"Bharti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02723962_CR1","first-page":"968","volume":"67","author":"JM Opitz","year":"1965","unstructured":"Opitz JM, Smith DW, Summit RL. Hypertelorism and hypospadias (abst).J. Pediatr 1965; 67: 968.","journal-title":"J. Pediatr"},{"key":"BF02723962_CR2","first-page":"95","volume":"5","author":"JM Optz","year":"1969","unstructured":"Optz JMet al. The G syndrome of multiple congenital anomalies.Birth Defects 1969; 5: 95\u2013101.","journal-title":"Birth Defects"},{"key":"BF02723962_CR3","first-page":"86","volume":"5","author":"JM Opitz","year":"1969","unstructured":"Opitz JMet al. The BBB syndrome. Familial telecanthus with associated congenital anomalies.Birth Defects 1969; 5:86\u201394.","journal-title":"Birth Defects"},{"key":"BF02723962_CR4","doi-asserted-by":"crossref","first-page":"951","DOI":"10.1016\/S0022-5347(17)49961-7","volume":"132","author":"HN Noe","year":"1984","unstructured":"Noe HN, Peeden JN, Jerkin GR, Wilroy RS Jr. Hypertelorism-hypospadias syndrome.J. Urol. 1984; 132:951\u2013952.","journal-title":"J. Urol."},{"key":"BF02723962_CR5","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1002\/ajmg.1320280207","volume":"28","author":"M Cappa","year":"1987","unstructured":"Cappa M, Borrelli P, Marini R, Neri G. The Opitz syndrome: A new designation for the clinically indistinguishable BBB and G syndrome.Am J Med Genet 1987; 28:303\u2013309.","journal-title":"Am J Med Genet"},{"key":"BF02723962_CR6","doi-asserted-by":"crossref","first-page":"145","DOI":"10.1002\/ajmg.1320020205","volume":"2","author":"JF Cordero","year":"1978","unstructured":"Cordero JF, Holmes LB. Phenotypic overlap of the BBB and G syndrome.Am J Med Genet 1978; 2:145\u2013152.","journal-title":"Am J Med Genet"},{"key":"BF02723962_CR7","first-page":"792","volume-title":"Syndromes of the Head and Neck","year":"1990","unstructured":"Corlin RJ, Pindborn JJ, Cohen MM, Levin LS (eds).Syndromes of the Head and Neck. New York; Oxford University Press 1990; 792\u2013796."},{"key":"BF02723962_CR8","doi-asserted-by":"crossref","first-page":"459","DOI":"10.1038\/ng1295-459","volume":"11","author":"NH Robin","year":"1995","unstructured":"Robin NH, Feldman GJ, Aronson Alet al. Opitz syndrome is genetically heterogenous, with one locus on Xp22 and a second locus on 22qll.2.Nat Genet 1995; 11:459\u2013461.","journal-title":"Nat Genet"},{"key":"BF02723962_CR9","first-page":"132","volume-title":"Smith\u2019s Recognizable Pattern of Human Malformations","author":"KL Jones","year":"1997","unstructured":"Jones KL.Smith\u2019s Recognizable Pattern of Human Malformations. Philadelphia; WB Saunders company, 1997; 132\u2013135."},{"key":"BF02723962_CR10","doi-asserted-by":"crossref","first-page":"24","DOI":"10.1016\/S1010-5182(05)80192-1","volume":"20","author":"JF Bershof","year":"1992","unstructured":"Bershof JF, Guyuron B, Olsen MM. G syndrome. A review of literature and a case report.J. Craniomaxillofac Surg 1992; 20: 24\u201377.","journal-title":"J. Craniomaxillofac Surg"},{"key":"BF02723962_CR11","doi-asserted-by":"crossref","first-page":"157","DOI":"10.1136\/jmg.25.3.157","volume":"25","author":"GN Wilson","year":"1988","unstructured":"Wilson GN, Oliver WD. Further delineation of the G syndrome. A manageable genetic cause of infantile dysphagia.J Med Genetic 1988; 25:157\u2013163.","journal-title":"J Med Genetic"},{"key":"BF02723962_CR12","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1016\/0165-5876(82)90047-7","volume":"4","author":"CP Kimmelman","year":"1982","unstructured":"Kimmelman CP, Denney JC. Opitz (G) syndrome.Int J Pediatr Otorhinolaryngol 1982; 4:343\u2013347.","journal-title":"Int J Pediatr Otorhinolaryngol"},{"key":"BF02723962_CR13","doi-asserted-by":"crossref","first-page":"1056","DOI":"10.1017\/S0022215100107261","volume":"102","author":"JG Buckley","year":"1988","unstructured":"Buckley JG, Hinton AE, Penter G, Farndon PA. Total laryngotracheal hypoplasia in a case of a G syndrome.J. Laryngol Otol 1988; 102:1056\u20131059.","journal-title":"J. Laryngol Otol"},{"key":"BF02723962_CR14","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1177\/000348948909800304","volume":"98","author":"L Howell","year":"1989","unstructured":"Howell L, Smith JD. G syndrome and its otolaryngologic manifestations.Ann Otol Rhinol Laryngol 1989; 98:185\u2013190.","journal-title":"Ann Otol Rhinol Laryngol"},{"key":"BF02723962_CR15","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1136\/thx.53.2.149","volume":"53","author":"D Sliva De","year":"1998","unstructured":"De Sliva D, Osborne A, Simpson SA, Dean JC, Seaton A. Opitz oculogenito-laryngeal syndrome. Arare cause of recurrent aspiration pneumonia in an adult.Thorax 1998; 53:149\u2013150.","journal-title":"Thorax"}],"container-title":["The Indian Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02723962.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02723962\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02723962","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,18]],"date-time":"2019-05-18T22:02:41Z","timestamp":1558216961000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02723962"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,12]]},"references-count":15,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2000,12]]}},"alternative-id":["BF02723962"],"URL":"https:\/\/doi.org\/10.1007\/bf02723962","relation":{},"ISSN":["0019-5456","0973-7693"],"issn-type":[{"value":"0019-5456","type":"print"},{"value":"0973-7693","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,12]]}}}