{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,26]],"date-time":"2026-03-26T17:46:28Z","timestamp":1774547188538,"version":"3.50.1"},"reference-count":12,"publisher":"Oxford University Press (OUP)","issue":"6","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":639,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Br J Dermatol"],"published-print":{"date-parts":[[2013,12]]},"DOI":"10.1111\/bjd.12458","type":"journal-article","created":{"date-parts":[[2013,6,8]],"date-time":"2013-06-08T06:11:32Z","timestamp":1370671892000},"page":"1342-1345","source":"Crossref","is-referenced-by-count":43,"title":["Molecular evidence of type 2 mosaicism in Gorlin syndrome"],"prefix":"10.1093","volume":"169","author":[{"given":"A.","family":"Torrelo","sequence":"first","affiliation":[{"name":"Department of Dermatology ; Hospital del Ni\u00f1o Jes\u00fas; Menendez Pelayo 65 Madrid 28034 Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Hern\u00e1ndez-Mart\u00edn","sequence":"additional","affiliation":[{"name":"Department of Dermatology ; Hospital del Ni\u00f1o Jes\u00fas; Menendez Pelayo 65 Madrid 28034 Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E.","family":"Bueno","sequence":"additional","affiliation":[{"name":"Department of Medicine; IBMCC and IBSAL; Universidad de Salamanca-CSIC; Salamanca Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Colmenero","sequence":"additional","affiliation":[{"name":"Department of Pathology; Hospital del Ni\u00f1o Jes\u00fas; Menendez Pelayo 65 Madrid 28034 Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Rivera","sequence":"additional","affiliation":[{"name":"Department of Dermatology ; Hospital del Ni\u00f1o Jes\u00fas; Menendez Pelayo 65 Madrid 28034 Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Requena","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Fundaci\u00f3n Jim\u00e9nez D\u00edaz; Madrid Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Happle","sequence":"additional","affiliation":[{"name":"Department of Dermatology; Freiburg University Medical Center; Freiburg Germany"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R.","family":"Gonz\u00e1lez-Sarmiento","sequence":"additional","affiliation":[{"name":"Department of Medicine; IBMCC and IBSAL; Universidad de Salamanca-CSIC; Salamanca Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[2013,12,2]]},"reference":[{"key":"10.1111\/bjd.12458-BIB0001|bjd12458-cit-0001","doi-asserted-by":"crossref","first-page":"1505","DOI":"10.1001\/archderm.1997.03890480025004","article-title":"A rule concerning the segmental manifestation of autosomal dominant skin disorders. Review of clinical examples providing evidence for dichotomous types of severity","volume":"133","author":"Happle","year":"1997","journal-title":"Arch Dermatol"},{"issue":"Suppl. 1","key":"10.1111\/bjd.12458-BIB0002|bjd12458-cit-0002","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1016\/S0001-7310(09)73171-0","article-title":"Superimposed segmental manifestation of both rare and common cutaneous disorders: a new paradigm","volume":"100","author":"Happle","year":"2009","journal-title":"Actas Dermosifiliogr"},{"key":"10.1111\/bjd.12458-BIB0003|bjd12458-cit-0003","doi-asserted-by":"crossref","first-page":"1467","DOI":"10.1172\/JCI21791","article-title":"Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept","volume":"114","author":"Poblete-Guti\u00e9rrez","year":"2004","journal-title":"J Clin Invest"},{"key":"10.1111\/bjd.12458-BIB0004|bjd12458-cit-0004","doi-asserted-by":"crossref","first-page":"464","DOI":"10.1111\/j.1365-2133.2011.10593.x","article-title":"Molecular genetic support for the rule of dichotomy in type 2 segmental Darier disease","volume":"166","author":"F\u00f6lster-Holst","year":"2012","journal-title":"Br J Dermatol"},{"key":"10.1111\/bjd.12458-BIB0005|bjd12458-cit-0005","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1097\/01.GIM.0000144188.15902.C4","article-title":"Nevoid basal cell carcinoma (Gorlin) syndrome","volume":"6","author":"Gorlin","year":"2004","journal-title":"Genet Med"},{"key":"10.1111\/bjd.12458-BIB0006|bjd12458-cit-0006","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1001\/archderm.1969.01610300091016","article-title":"Quadrant distribution of basal cell nevi","volume":"100","author":"Shelley","year":"1969","journal-title":"Arch Dermatol"},{"key":"10.1111\/bjd.12458-BIB0007|bjd12458-cit-0007","doi-asserted-by":"crossref","first-page":"365","DOI":"10.1111\/j.1365-2133.1985.tb02092.x","article-title":"Naevoid basal-cell carcinoma syndrome with unilateral neoplasms and pits","volume":"113","author":"Camisa","year":"1985","journal-title":"Br J Dermatol"},{"key":"10.1111\/bjd.12458-BIB0008|bjd12458-cit-0008","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1038\/ng0196-85","article-title":"A two-hit model for developmental defects in Gorlin syndrome","volume":"12","author":"Levanat","year":"1996","journal-title":"Nat Genet"},{"key":"10.1111\/bjd.12458-BIB0009|bjd12458-cit-0009","doi-asserted-by":"crossref","first-page":"382","DOI":"10.2340\/00015555-0495","article-title":"Segmentally arranged basaloid follicular hamartomas with osseous, and cerebral anomalies: a distinct syndrome","volume":"88","author":"Happle","year":"2008","journal-title":"Acta Derm Venereol"},{"key":"10.1111\/bjd.12458-BIB0010|bjd12458-cit-0010","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1159\/000174103","article-title":"Happle-Tinschert syndrome. Segmentally arranged basaloid follicular hamartomas, linear atrophoderma with hypo- and hyperpigmentation, enamel defects, ipsilateral hypertrichosis, and skeletal and cerebral anomalies","volume":"218","author":"Itin","year":"2009","journal-title":"Dermatology"},{"key":"10.1111\/bjd.12458-BIB0011|bjd12458-cit-0011","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1111\/j.1525-1470.2010.01225.x","article-title":"Congenital systematized basaloid follicular hamartoma with microphthalmia and hemimegalencephaly","volume":"28","author":"Boccaletti","year":"2011","journal-title":"Pediatr Dermatol"},{"key":"10.1111\/bjd.12458-BIB0012|bjd12458-cit-0012","doi-asserted-by":"crossref","first-page":"e17","DOI":"10.1016\/j.jaad.2010.12.010","article-title":"A novel phenotype with features of basal cell nevus syndrome and basaloid follicular hamartoma syndrome","volume":"65","author":"Waxweiler","year":"2011","journal-title":"J Am Acad Dermatol"}],"container-title":["British Journal of Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fbjd.12458","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/bjd.12458\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,7,2]],"date-time":"2023-07-02T08:13:11Z","timestamp":1688285591000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/bjd\/article\/169\/6\/1342\/6615132"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,12]]},"references-count":12,"journal-issue":{"issue":"6","published-print":{"date-parts":[[2013,12]]}},"URL":"https:\/\/doi.org\/10.1111\/bjd.12458","relation":{},"ISSN":["0007-0963"],"issn-type":[{"value":"0007-0963","type":"print"}],"subject":[],"published":{"date-parts":[[2013,12]]}}}