{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T16:07:54Z","timestamp":1790698074462,"version":"4.1.0"},"reference-count":10,"publisher":"Elsevier BV","issue":"5","license":[{"start":{"date-parts":[[2012,5,1]],"date-time":"2012-05-01T00:00:00Z","timestamp":1335830400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Brain and Development"],"published-print":{"date-parts":[[2012,5]]},"DOI":"10.1016\/j.braindev.2011.07.011","type":"journal-article","created":{"date-parts":[[2011,8,31]],"date-time":"2011-08-31T22:19:39Z","timestamp":1314829179000},"page":"392-395","source":"Crossref","is-referenced-by-count":9,"title":["Pontocerebellar hypoplasia type 3 with tetralogy of Fallot"],"prefix":"10.1016","volume":"34","author":[{"given":"Hideo","family":"Jinnou","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tohru","family":"Okanishi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hideo","family":"Enoki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shigeru","family":"Ohki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.braindev.2011.07.011_b0005","doi-asserted-by":"crossref","first-page":"411","DOI":"10.1016\/0387-7604(93)90080-R","article-title":"Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset","volume":"15","author":"Barth","year":"1993","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2011.07.011_b0010","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1053\/ejpn.2000.0294","article-title":"Pontocerebellar hypoplasia \u2013 How many types?","volume":"4","author":"Barth","year":"2000","journal-title":"Eur J Paediatr Neurol"},{"key":"10.1016\/j.braindev.2011.07.011_b0015","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1212\/WNL.45.2.311","article-title":"The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigrees","volume":"45","author":"Barth","year":"1995","journal-title":"Neurology"},{"key":"10.1016\/j.braindev.2011.07.011_b0020","doi-asserted-by":"crossref","first-page":"1664","DOI":"10.1212\/01.WNL.0000068548.58498.41","article-title":"A novel form of pontocerebellar hypoplasia maps to chromosome 7q11\u201321","volume":"60","author":"Rajab","year":"2003","journal-title":"Neurology"},{"key":"10.1016\/j.braindev.2011.07.011_b0025","doi-asserted-by":"crossref","first-page":"394","DOI":"10.1007\/BF00334450","article-title":"Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings","volume":"85","author":"Albrecht","year":"1993","journal-title":"Acta Neuropathol"},{"key":"10.1016\/j.braindev.2011.07.011_b0030","doi-asserted-by":"crossref","first-page":"414","DOI":"10.1016\/j.ygeno.2009.08.015","article-title":"TULIP1 (RALGAPA1) haploinsufficiency with brain development delay","volume":"94","author":"Shimojima","year":"2009","journal-title":"Genomics"},{"key":"10.1016\/j.braindev.2011.07.011_b0035","doi-asserted-by":"crossref","first-page":"416","DOI":"10.1007\/s00415-009-0094-0","article-title":"Pontocerebellar hypoplasia type III (CLAM): extended phenotype and novel molecular findings","volume":"256","author":"Durmaz","year":"2009","journal-title":"J Neurol"},{"key":"10.1016\/j.braindev.2011.07.011_b0040","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1136\/jmg.2009.070391","article-title":"Comprehensive genotype\u2013phenotype analysis in 230 patients with tetralogy of Fallot","volume":"47","author":"Rauch","year":"2010","journal-title":"J Med Genet"},{"key":"10.1016\/j.braindev.2011.07.011_b0045","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1016\/j.pediatrneurol.2010.09.002","article-title":"Pontocerebellar hypoplasia type 3 with severe vitamin A deficiency","volume":"44","author":"Jacob","year":"2011","journal-title":"Pediatr Neurol"},{"key":"10.1016\/j.braindev.2011.07.011_b0050","doi-asserted-by":"crossref","first-page":"961","DOI":"10.1096\/fasebj.10.9.8801178","article-title":"Embryonic development and pattern formation","volume":"10","author":"Morriss-Kay","year":"1996","journal-title":"FASEB J"}],"container-title":["Brain and Development"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0387760411002087?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0387760411002087?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,6,14]],"date-time":"2019-06-14T18:00:22Z","timestamp":1560535222000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0387760411002087"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,5]]},"references-count":10,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2012,5]]}},"alternative-id":["S0387760411002087"],"URL":"https:\/\/doi.org\/10.1016\/j.braindev.2011.07.011","relation":{},"ISSN":["0387-7604"],"issn-type":[{"value":"0387-7604","type":"print"}],"subject":[],"published":{"date-parts":[[2012,5]]}}}