{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T12:35:14Z","timestamp":1759667714712},"reference-count":6,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,1]]},"DOI":"10.1097\/mcd.0000000000000202","type":"journal-article","created":{"date-parts":[[2017,8,31]],"date-time":"2017-08-31T17:15:27Z","timestamp":1504199727000},"page":"23-24","source":"Crossref","is-referenced-by-count":2,"title":["Arytenoid neuromas are a recognized feature of SOS1 mutations causing pure mucosal neuroma syndrome"],"prefix":"10.1097","volume":"27","author":[{"given":"Peter J.","family":"Leyden","sequence":"first","affiliation":[{"name":"Department of ENT, Craigavon Area Hospital, Portadown"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Patrick J.","family":"Morrison","sequence":"additional","affiliation":[{"name":"Department of Genetic Medicine, Belfast Health and Social Care Trust, UK"},{"name":"Centre for Cancer Research and Cell Biology, Queens University Belfast, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-20230915","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1093\/hmg\/3.2.237","article-title":"Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours","volume":"3","author":"Eng","year":"1994","journal-title":"Hum Mol Genet"},{"key":"R2-20230915","doi-asserted-by":"crossref","first-page":"943","DOI":"10.1086\/339689","article-title":"A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1","volume":"70","author":"Hart","year":"2002","journal-title":"Am J Hum Genet"},{"key":"R3-20230915","doi-asserted-by":"crossref","first-page":"715","DOI":"10.1111\/cen.13008","article-title":"SOS1 frameshift mutations cause pure mucosal neuroma syndrome, a clinical phenotype distinct from multiple endocrine neoplasia type 2B","volume":"84","author":"Owens","year":"2016","journal-title":"Clin Endocrinol"},{"key":"R4-20230915","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1016\/S0190-9622(97)80390-8","article-title":"Multiple idiopathic mucosal neuromas: a minor form of multiple endocrine neoplasia type 2B or a new entity","volume":"37","author":"Pujol","year":"1997","journal-title":"J Am Acads Dermatol"},{"key":"R5-20230915","doi-asserted-by":"crossref","first-page":"333","DOI":"10.1016\/S0140-6736(12)61023-X","article-title":"Noonan syndrome","volume":"381","author":"Roberts","year":"2013","journal-title":"Lancet"},{"key":"R7-20230915","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1016\/S0092-8674(00)00026-X","article-title":"The EGF receptor provides an essential survival signal for SOS-dependent skin tumor development","volume":"102","author":"Sibilia","year":"2000","journal-title":"Cell"}],"container-title":["Clinical Dysmorphology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/00019605-201801000-00009","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,15]],"date-time":"2023-09-15T20:03:27Z","timestamp":1694808207000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00019605-201801000-00009"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,1]]},"references-count":6,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2018]]}},"URL":"https:\/\/doi.org\/10.1097\/mcd.0000000000000202","relation":{},"ISSN":["0962-8827"],"issn-type":[{"value":"0962-8827","type":"print"}],"subject":[],"published":{"date-parts":[[2018,1]]}}}