{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,31]],"date-time":"2025-12-31T12:31:42Z","timestamp":1767184302828,"version":"build-2238731810"},"reference-count":6,"publisher":"American Academy of Pediatrics (AAP)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2012,3,1]]},"DOI":"10.1542\/pir.33.3.e18","type":"journal-article","created":{"date-parts":[[2021,12,11]],"date-time":"2021-12-11T01:37:20Z","timestamp":1639186640000},"page":"e18-e21","source":"Crossref","is-referenced-by-count":2,"title":["A Male Infant Who Has A White Hair Tuft and Hypopigmented Macules"],"prefix":"10.1542","volume":"33","author":[{"given":"Joshua","family":"Wong","sequence":"first","affiliation":[{"name":"Advocate, Hope Children's Hospital, Oak Lawn, IL."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"417","published-online":{"date-parts":[[2012,3,1]]},"reference":[{"issue":"2","key":"2021121020483722000_B1","first-page":"384","article-title":"Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome","volume":"58","author":"Reynolds","year":"1996","journal-title":"Am J Hum Genet"},{"issue":"5","key":"2021121020483722000_B2","first-page":"902","article-title":"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","volume":"50","author":"Farrer","year":"1992","journal-title":"Am J Hum Genet"},{"key":"2021121020483722000_B3","volume-title":"Smith's Recognizable Patterns of Human Malformation","author":"Jones","year":"2006","edition":"6th ed."},{"issue":"3","key":"2021121020483722000_B4","first-page":"21","article-title":"Waardenburg syndrome type 1","volume":"12","author":"Karaman","year":"2006","journal-title":"Dermatol Online J"},{"issue":"1","key":"2021121020483722000_B5","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1002\/ajmg.1320550123","article-title":"Waardenburg syndrome type II: phenotypic findings and diagnostic criteria","volume":"55","author":"Liu","year":"1995","journal-title":"Am J Med Genet"},{"issue":"4","key":"2021121020483722000_B6","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1002\/humu.21211","article-title":"Review and update of mutations causing Waardenburg syndrome","volume":"31","author":"Pingault","year":"2010","journal-title":"Hum Mutat"}],"container-title":["Pediatrics In Review"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/publications.aap.org\/pediatricsinreview\/article-pdf\/33\/3\/e18\/823962\/pedsinreview_2012024.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/publications.aap.org\/pediatricsinreview\/article-pdf\/33\/3\/e18\/823962\/pedsinreview_2012024.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,12,21]],"date-time":"2021-12-21T09:39:32Z","timestamp":1640079572000},"score":1,"resource":{"primary":{"URL":"https:\/\/publications.aap.org\/pediatricsinreview\/article\/33\/3\/e18\/34704\/A-Male-Infant-Who-Has-A-White-Hair-Tuft-and"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,3,1]]},"references-count":6,"aliases":["10.1542\/pir.33-3-e18"],"journal-issue":{"issue":"3","published-online":{"date-parts":[[2012,3,1]]},"published-print":{"date-parts":[[2012,3,1]]}},"URL":"https:\/\/doi.org\/10.1542\/pir.33.3.e18","relation":{},"ISSN":["0191-9601","1526-3347"],"issn-type":[{"value":"0191-9601","type":"print"},{"value":"1526-3347","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,3,1]]}}}