{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T05:50:37Z","timestamp":1790833837707,"version":"4.1.0"},"reference-count":20,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2011,4,11]],"date-time":"2011-04-11T00:00:00Z","timestamp":1302480000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2011,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p><jats:italic>WNT10A<\/jats:italic> has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive Sch\u00d6pf\u2013Schulz\u2013Passarge syndrome to odonto\u2010onycho\u2010dermal dysplasia and autosomal dominant hypodontia. We report <jats:italic>WNT10A<\/jats:italic> mutations in an American family of which four members are affected with isolated hypodontia or microdontia. Here we demonstrate that in addition to <jats:italic>MSX1, PAX9, AXIN2<\/jats:italic>, and <jats:italic>EDA<\/jats:italic>, mutations in <jats:italic>WNT10A<\/jats:italic> can cause isolated hypodontia. \u00a9 2011 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.33840","type":"journal-article","created":{"date-parts":[[2011,4,11]],"date-time":"2011-04-11T15:08:45Z","timestamp":1302534525000},"page":"1119-1122","source":"Crossref","is-referenced-by-count":82,"title":["<i>WNT10A<\/i> and isolated hypodontia"],"prefix":"10.1002","volume":"155","author":[{"given":"Piranit","family":"Kantaputra","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Warissara","family":"Sripathomsawat","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2011,4,11]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1086\/520064"},{"key":"e_1_2_5_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2009.06.001"},{"key":"e_1_2_5_4_1","doi-asserted-by":"crossref","first-page":"607","DOI":"10.2340\/00015555-0547","article-title":"Sch\u00f6pf\u2013Schulz\u2013Passarge syndrome: Further delineation of the phenotype and genetic considerations","volume":"88","author":"Castori M","year":"2008","journal-title":"Acta Derm Venereol"},{"key":"e_1_2_5_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.20473"},{"key":"e_1_2_5_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.31368"},{"key":"e_1_2_5_7_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320140213"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1002\/dvdy.21156"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.1101\/gad.1035602"},{"key":"e_1_2_5_10_1","doi-asserted-by":"publisher","DOI":"10.1086\/386293"},{"key":"e_1_2_5_11_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ydbio.2007.10.016"},{"key":"e_1_2_5_12_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.30188"},{"key":"e_1_2_5_13_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jdermsci.2010.03.012"},{"key":"e_1_2_5_14_1","doi-asserted-by":"publisher","DOI":"10.1002\/dvdy.20321"},{"key":"e_1_2_5_15_1","doi-asserted-by":"publisher","DOI":"10.1038\/ejhg.2009.81"},{"key":"e_1_2_5_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0925-4773(01)00452-X"},{"key":"e_1_2_5_17_1","first-page":"219","article-title":"Syndrome of cystic eyelids, palmo\u2010plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive trait","volume":"7","author":"Sch\u00f6pf E","year":"1971","journal-title":"Birth Defects Orig Artic Ser"},{"key":"e_1_2_5_18_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.31360"},{"key":"e_1_2_5_19_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2133.2010.09703.x"},{"key":"e_1_2_5_20_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1432-0436.2006.00150.x"},{"key":"e_1_2_5_21_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.devcel.2009.05.011"}],"container-title":["American Journal of Medical Genetics Part A"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.a.33840","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.a.33840","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.a.33840","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,14]],"date-time":"2023-09-14T07:54:08Z","timestamp":1694678048000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.a.33840"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,4,11]]},"references-count":20,"journal-issue":{"issue":"5","published-print":{"date-parts":[[2011,5]]}},"alternative-id":["10.1002\/ajmg.a.33840"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.a.33840","archive":["Portico"],"relation":{},"ISSN":["1552-4825","1552-4833"],"issn-type":[{"value":"1552-4825","type":"print"},{"value":"1552-4833","type":"electronic"}],"subject":[],"published":{"date-parts":[[2011,4,11]]}}}