{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,4,5]],"date-time":"2022-04-05T06:22:17Z","timestamp":1649139737195},"reference-count":10,"publisher":"Springer Science and Business Media LLC","issue":"7","license":[{"start":{"date-parts":[[2009,12,20]],"date-time":"2009-12-20T00:00:00Z","timestamp":1261267200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ophthalmologe"],"published-print":{"date-parts":[[2010,7]]},"DOI":"10.1007\/s00347-009-2084-0","type":"journal-article","created":{"date-parts":[[2009,12,18]],"date-time":"2009-12-18T13:54:27Z","timestamp":1261144467000},"page":"660-662","source":"Crossref","is-referenced-by-count":0,"title":["Blickdiagnose"],"prefix":"10.1007","volume":"107","author":[{"given":"T.","family":"Hager","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.-S.","family":"Walter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"Seitz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"K\u00e4smann-Kellner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2009,12,20]]},"reference":[{"key":"2084_CR1","first-page":"103","volume":"26","author":"Arias","year":"1978","unstructured":"Arias S, Mota M (1978) Apparent non-penetrance for dystopia in Waardenburg syndrome type I, with some hints on the diagnosis of dystopia canthorum. J Genet Hum 26:103\u2013131","journal-title":"J Genet Hum"},{"key":"2084_CR2","doi-asserted-by":"crossref","first-page":"719","DOI":"10.1258\/0022215054797943","volume":"119","author":"Daneshi","year":"2005","unstructured":"Daneshi A, Hassanzadeh S, Farhadi M (2005) Cochlear implantation in children with Waardenburg syndrome. J Laryngol Otol 119(9):719\u2013723","journal-title":"J Laryngol Otol"},{"key":"2084_CR3","first-page":"902","volume":"50","author":"Farrer","year":"1992","unstructured":"Farrer LA, Grundfast KM, Amos J (1992) Waardenburg syndrome (WS) type I is caused by defects at multiple loci one of which is near ALPP on chromosome 2: first report of the WS consortium. Am J Hum Genet 50:902\u2013913","journal-title":"Am J Hum Genet"},{"key":"2084_CR4","doi-asserted-by":"crossref","first-page":"2107","DOI":"10.1126\/science.280.5372.2107","volume":"280","author":"Fleming","year":"1998","unstructured":"Fleming A, Copp AJ (1998) Embryonic folate metabolism and mouse neural tube defects. Science 280(5372):2107\u20132109","journal-title":"Science"},{"key":"2084_CR5","first-page":"799","volume":"22","author":"Mouriaux","year":"1999","unstructured":"Mouriaux F, Hamedani M, Hurbli T et al (1999) Le syndrome de Waardenburg. J Fr Ophtalmol 22(7):799\u2013809","journal-title":"J Fr Ophtalmol"},{"key":"2084_CR6","first-page":"201","volume":"61","author":"Newton","year":"2002","unstructured":"Newton VE (2002) Clinical features of the Waardenburg syndromes. Adv Otorhinolaryngol 61:201\u2013208","journal-title":"Adv Otorhinolaryngol"},{"key":"2084_CR7","doi-asserted-by":"crossref","first-page":"656","DOI":"10.1136\/jmg.34.8.656","volume":"34","author":"Read","year":"1997","unstructured":"Read AP, Newton VE (1997) Waardenburg syndrome. J Med Genet 34:656\u2013665","journal-title":"J Med Genet"},{"key":"2084_CR8","first-page":"725","volume":"63","author":"Sellars","year":"1983","unstructured":"Sellars S, Beighton P (1983) The Waardenburg syndrome in deaf children in southern Africa. S Afr Med J 63:725\u2013728","journal-title":"S Afr Med J"},{"key":"2084_CR9","doi-asserted-by":"crossref","first-page":"201","DOI":"10.1620\/tjem.211.201","volume":"211","author":"Takeda","year":"2007","unstructured":"Takeda K, Takahashi NH, Shibahafra S (2007) Neuroendocrine functions of melanocytes: beyond the skin-deep melanin marker. Tohoku J Exp Med 211:201\u2013221","journal-title":"Tohoku J Exp Med"},{"key":"2084_CR10","doi-asserted-by":"crossref","first-page":"42","DOI":"10.1002\/ajmg.a.20260","volume":"122","author":"Wollnik","year":"2003","unstructured":"Wollnik B, Tukel T, Uyguner O et al (2003) Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome. Am J Med Genet A 122(1):42\u201345","journal-title":"Am J Med Genet A"}],"container-title":["Der Ophthalmologe"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00347-009-2084-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00347-009-2084-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00347-009-2084-0","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,28]],"date-time":"2019-05-28T13:50:58Z","timestamp":1559051458000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00347-009-2084-0"}},"subtitle":["Waardenburg-Syndrom"],"short-title":[],"issued":{"date-parts":[[2009,12,20]]},"references-count":10,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2010,7]]}},"alternative-id":["2084"],"URL":"https:\/\/doi.org\/10.1007\/s00347-009-2084-0","relation":{},"ISSN":["0941-293X","1433-0423"],"issn-type":[{"value":"0941-293X","type":"print"},{"value":"1433-0423","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,12,20]]}}}