{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T13:46:58Z","timestamp":1768484818155,"version":"3.49.0"},"reference-count":9,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":532,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clin Exp Dermatol"],"published-print":{"date-parts":[[2014,4]]},"DOI":"10.1111\/ced.12272","type":"journal-article","created":{"date-parts":[[2014,3,18]],"date-time":"2014-03-18T06:44:40Z","timestamp":1395125080000},"page":"310-314","source":"Crossref","is-referenced-by-count":10,"title":["X-linked dyskeratosis congenita presenting in adulthood with photodamaged skin and epiphora"],"prefix":"10.1093","volume":"39","author":[{"given":"J. B.","family":"Powell","sequence":"first","affiliation":[{"name":"Department of Dermatology; Worcestershire Royal Hospital; Worcester UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Dokal","sequence":"additional","affiliation":[{"name":"Blizard Institute; Barts and The London School of Medicine and Dentistry; London UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Carr","sequence":"additional","affiliation":[{"name":"Department of Histopathology; Warwick Hospital; Warwick UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Taibjee","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Birmingham Children's Hospital; UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B.","family":"Cave","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Birmingham Children's Hospital; UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Moss","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Birmingham Children's Hospital; UK"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2014,3,18]]},"reference":[{"key":"10.1111\/ced.12272-BIB0001|ced12272-cit-0001","doi-asserted-by":"crossref","first-page":"480","DOI":"10.1182\/asheducation-2011.1.480","article-title":"Dyskeratosis congenita","volume":"2011","author":"Dokal","year":"2011","journal-title":"Hematology Am Soc Hematol Educ Program"},{"key":"10.1111\/ced.12272-BIB0002|ced12272-cit-0002","doi-asserted-by":"crossref","first-page":"2680","DOI":"10.1182\/blood-2005-07-2622","article-title":"Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation","volume":"107","author":"Vulliamy","year":"2006","journal-title":"Blood"},{"key":"10.1111\/ced.12272-BIB0003|ced12272-cit-0003","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1046\/j.1365-2141.1999.01690.x","article-title":"Unexplained aplastic anaemia, immunodeficiency and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) is caused by mutations in the DKC1 gene","volume":"107","author":"Knight","year":"1999","journal-title":"Br J Haematol"},{"key":"10.1111\/ced.12272-BIB0004|ced12272-cit-0004","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1136\/jmg.29.9.673","article-title":"Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?","volume":"29","author":"Revesz","year":"1992","journal-title":"J Med Genet"},{"key":"10.1111\/ced.12272-BIB0005|ced12272-cit-0005","doi-asserted-by":"crossref","first-page":"448","DOI":"10.1016\/j.ajhg.2013.02.001","article-title":"Constitutional mutations in RTEL1 cause severe dyskeratosis congenita","volume":"92","author":"Walne","year":"2013","journal-title":"Am J Hum Genet"},{"key":"10.1111\/ced.12272-BIB0006|ced12272-cit-0006","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1016\/j.mrfmmm.2011.06.008","article-title":"Dyskeratosis congenital as a disorder of telomere maintenance","volume":"1730","author":"Nelson","year":"2012","journal-title":"Mutat Res"},{"key":"10.1111\/ced.12272-BIB0007|ced12272-cit-0007","doi-asserted-by":"crossref","first-page":"353","DOI":"10.3324\/haematol.2011.055269","article-title":"Telomere length is associated with disease severity and declines with age in dyskeratosis congenita","volume":"97","author":"Alter","year":"2012","journal-title":"Haematologica"},{"key":"10.1111\/ced.12272-BIB0008|ced12272-cit-0008","first-page":"201","article-title":"Progression of actinic keratosis to squamous cell carcinoma revisited: clinical and treatment implications","volume":"87","author":"Feldman","year":"2011","journal-title":"Cutis"},{"key":"10.1111\/ced.12272-BIB0009|ced12272-cit-0009","doi-asserted-by":"crossref","first-page":"6549","DOI":"10.1182\/blood-2008-12-192880","article-title":"Cancer in dyskeratosis congenita","volume":"113","author":"Alter","year":"2009","journal-title":"Blood"}],"container-title":["Clinical and Experimental Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fced.12272","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/ced.12272\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,2,14]],"date-time":"2023-02-14T14:38:53Z","timestamp":1676385533000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/ced\/article\/39\/3\/310\/6621264"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,3,18]]},"references-count":9,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2014,4]]}},"URL":"https:\/\/doi.org\/10.1111\/ced.12272","relation":{},"ISSN":["0307-6938"],"issn-type":[{"value":"0307-6938","type":"print"}],"subject":[],"published":{"date-parts":[[2014,3,18]]}}}