{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,8,3]],"date-time":"2024-08-03T18:20:41Z","timestamp":1722709241645},"reference-count":14,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,9]],"date-time":"2005-06-09T00:00:00Z","timestamp":1118275200000},"content-version":"vor","delay-in-days":3629,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1995,7,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report on an 8\u2010year\u2010old Japanese boy with Setleis syndrome. The patient had a very characteristic \u201ccoarse\u201d facial appearance, bitemporal \u201cforceps marks,\u201d skin aplasia, sparse hair, and skin hypo\u2010 and hy\u2010perpigmentation. He also had previously undescribed manifestations, including an aberrant hair pattern of the forehead, linear skin lesions on the forehead, short palpebral fissures, a small skin tag on the right cheek, cone\u2010shaped teeth, and pectus carinatum. Dermatoglyphic studies documented aberrant distal palmar creases (simian crease variant), 8 arches, and reduced total finger ridge count. When serial photographs were reviewed, his facial characteristics became more obvious with increasing age. \u00a9 1995 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.1320570316","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T18:03:27Z","timestamp":1118513007000},"page":"444-446","source":"Crossref","is-referenced-by-count":8,"title":["Follow\u2010up study in a patient with Setleis syndrome"],"prefix":"10.1002","volume":"57","author":[{"given":"Masato","family":"Tsukahara","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takahiro","family":"Okabe","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Morimasa","family":"Ohtsuka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Susumu","family":"Furukawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,9]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1097\/00019605-199207000-00006"},{"key":"e_1_2_1_3_1","first-page":"1163","article-title":"Hereditarer symmetrischer systematisierter Naevus aplasticus bei 38 Personen","volume":"89","author":"Brauer A","year":"1929","journal-title":"Dermatol Wochenschr"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320340311"},{"key":"e_1_2_1_5_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1986.tb01258.x"},{"key":"e_1_2_1_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/0190-9622(91)70211-J"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(73)91291-9"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(88)70125-5"},{"key":"e_1_2_1_9_1","first-page":"895","article-title":"Autosomal recessive inheritance in the Setleis bitemporal \u201cforceps marks\u201d syndrome","volume":"141","author":"Marion RW","year":"1987","journal-title":"Am J Dis Child"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1442-200X.1991.tb01541.x"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1973.01620190063015"},{"key":"e_1_2_1_12_1","doi-asserted-by":"crossref","first-page":"615","DOI":"10.1001\/archderm.1974.01630100071018","article-title":"Bitemporal aplasia cutis congenita: occurrence with other cutaneous abnormalities","volume":"110","author":"Rudolph RI","year":"1974","journal-title":"Arch Dermatol"},{"key":"e_1_2_1_13_1","doi-asserted-by":"crossref","first-page":"636","DOI":"10.1001\/archderm.1974.01630100084027","article-title":"Emendation to \u201cbitemporal aplasia cutis congenita","volume":"110","author":"Rudolph RI","year":"1974","journal-title":"Arch Dermatol"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.32.4.540"},{"key":"e_1_2_1_15_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(73)80258-6"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320570316","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320570316","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,26]],"date-time":"2023-10-26T07:29:40Z","timestamp":1698305380000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320570316"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1995,7,3]]},"references-count":14,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1995,7,3]]}},"alternative-id":["10.1002\/ajmg.1320570316"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320570316","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1995,7,3]]}}}