{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,27]],"date-time":"2023-10-27T04:56:40Z","timestamp":1698382600293},"reference-count":7,"publisher":"Springer Science and Business Media LLC","issue":"8","license":[{"start":{"date-parts":[[1990,10,1]],"date-time":"1990-10-01T00:00:00Z","timestamp":654739200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatr Radiol"],"published-print":{"date-parts":[[1990,10]]},"DOI":"10.1007\/bf02129073","type":"journal-article","created":{"date-parts":[[2005,9,14]],"date-time":"2005-09-14T15:43:38Z","timestamp":1126712618000},"page":"612-614","source":"Crossref","is-referenced-by-count":9,"title":["A new syndrome with cerebro-oculo-skeletal-renal involvement"],"prefix":"10.1007","volume":"20","author":[{"given":"M. C.","family":"Silengo","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Lerone","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Pelizza","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Gatti","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Barabino","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"Romeo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02129073_CR1","doi-asserted-by":"crossref","first-page":"556","DOI":"10.1016\/S0002-9343(70)80051-1","volume":"49","author":"F Mainzer","year":"1970","unstructured":"Mainzer F, Saldino R, Ozonoff MB, Minagi H (1970) Familial nephropathy associated with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities. Am J Med 49: 556","journal-title":"Am J Med"},{"key":"BF02129073_CR2","first-page":"375","volume":"82","author":"L Diekmann","year":"1977","unstructured":"Diekmann L, Louis C, Schulte-Kenna (1977) Familiale nephropathie mit retinitis pigmentosa und periphere dysostose. Helv Paediatr Acta 82:375","journal-title":"Helv Paediatr Acta"},{"key":"BF02129073_CR3","doi-asserted-by":"crossref","first-page":"238","DOI":"10.1007\/BF02388169","volume":"17","author":"M Cirillo Silengo","year":"1987","unstructured":"Cirillo Silengo M, Lopez Bell G, Biagioli M, Guala A, Porcellini G, Franceschini P (1987) A new syndrome with ocular, skeletal and renal involvement. Pediatr Radiol 17:238","journal-title":"Pediatr Radiol"},{"key":"BF02129073_CR4","doi-asserted-by":"crossref","first-page":"521","DOI":"10.1002\/ajmg.1320220310","volume":"22","author":"JM Opitz","year":"1985","unstructured":"Opitz JM, Lowry RS, Holmes TM, Morgan K (1985) Hutterite cerebro-osteo-nephrodysplasia: autosomal recessive trait in a Lehrerlut Hutterite family from Montana. Am J Med Genet 22:521","journal-title":"Am J Med Genet"},{"key":"BF02129073_CR5","doi-asserted-by":"crossref","first-page":"275","DOI":"10.1148\/89.2.275","volume":"89","author":"H Taybi","year":"1967","unstructured":"Taybi H, Linder D (1967) Congenital familial dwarfism with cephaloskeletal dysplasia. Radiology 89:275","journal-title":"Radiology"},{"key":"BF02129073_CR6","doi-asserted-by":"crossref","first-page":"37","DOI":"10.1002\/ajmg.1320120105","volume":"12","author":"F Majewski","year":"1982","unstructured":"Majewski F, Stoeckenius M, Kemperdich H (1982) Studies of microcephalic primordial dwarfism III. An intrauterine dwarf with platyspondyly and anomalies of pelvis and clavicles. Osteodysplastic primordial dwarfism type III. Am J Med Genet 12:37","journal-title":"Am J Med Genet"},{"key":"BF02129073_CR7","first-page":"57","volume":"41","author":"B Lavollay","year":"1984","unstructured":"Lavollay B, Faure C, Filipe G, Branca G, Huet De Barochez Y (1984) Nanisme familial congenital avec dysplasie cephalosquelettique. (Syndrome de Taybi-Linder) Arch Fr Pediatr 41:57","journal-title":"Arch Fr Pediatr"}],"container-title":["Pediatric Radiology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02129073.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02129073\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02129073","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,13]],"date-time":"2019-05-13T21:45:52Z","timestamp":1557783952000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02129073"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1990,10]]},"references-count":7,"journal-issue":{"issue":"8","published-print":{"date-parts":[[1990,10]]}},"alternative-id":["BF02129073"],"URL":"https:\/\/doi.org\/10.1007\/bf02129073","relation":{},"ISSN":["0301-0449","1432-1998"],"issn-type":[{"value":"0301-0449","type":"print"},{"value":"1432-1998","type":"electronic"}],"subject":[],"published":{"date-parts":[[1990,10]]}}}