{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,1,2]],"date-time":"2024-01-02T09:59:20Z","timestamp":1704189560338},"reference-count":12,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2005,6,2]],"date-time":"2005-06-02T00:00:00Z","timestamp":1117670400000},"content-version":"vor","delay-in-days":8918,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1981,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>The second of twin males expired of respiratory insufficiency shortly after birth. Unusual facial appearance included prominent forehead, flat nasal bridge, widely separated inner canthi, downward slanting eyes with narrow palpebral fissures, epicanthic folds, small mouth and micrognathia, and apparently low\u2010set ears; there was also cryptorchidism bilaterally and a simian crease bilaterally. The pregnancy of the 19\u2010year\u2010old black woman was not unusual, but polyhydramnios accompanied the delivery of this twin. The twin placentae were diamniotic and monochorionic, one being slightly immature with a two\u2010vessel cord. We interpreted the karyotype as 46,XY,del(10) (p11\u201315): The brother and parents were normal.<\/jats:p><jats:p>The dysmorphic features of this and three previously reported cases of 10p\u2010 do not permit definition of a syndrome.<\/jats:p><jats:p>These are apparently the first monozygous twins presenting discordance of chromosomal structure; previously reported chromosomal discordance in monozygous twins involved numerical abnormality. Considering that the mechanism of monozygous twinning is not understood, we note that the occurrence of both twinning and a structural aberration in one of the twins suggests the possibility of a common cause.<\/jats:p>","DOI":"10.1002\/ajmg.1320100213","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T17:39:07Z","timestamp":1118511547000},"page":"193-200","source":"Crossref","is-referenced-by-count":14,"title":["Clinicopathologic conference: A newborn monozygotic twin with abnormal facial appearance and respiratory insufficiency"],"prefix":"10.1002","volume":"10","author":[{"given":"Richard C.","family":"Juberg","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Richard","family":"Stallard","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"William J.","family":"Straughen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kosi J.","family":"Avotri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John W.","family":"Washington","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Enid F.","family":"Gilbert","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,6,2]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM197306142882406"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1977.tb07965.x"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1017\/S000156600001388X"},{"key":"e_1_2_1_5_1","first-page":"645","volume-title":"Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies","author":"Borgaonkar DS","year":"1980"},{"key":"e_1_2_1_6_1","first-page":"1","volume-title":"Clinical Atlas of Human Chromosomes","author":"de Grouchy J","year":"1977"},{"key":"e_1_2_1_7_1","first-page":"343","article-title":"Del(10)p autosomal deletion syndrome: Clinical, cytogenetic, and gene marker studies","volume":"26","author":"Francke U","year":"1975","journal-title":"Humangenetik"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1017\/S0001566000013817"},{"key":"e_1_2_1_9_1","first-page":"1","volume-title":"Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X\u2010linked Phenotypes","author":"McKusick VA","year":"1978"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00286969"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.12.1.99"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00282026"},{"key":"e_1_2_1_13_1","first-page":"1","volume-title":"New Chromosomal Syndromes","author":"Yunis JJ","year":"1977"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320100213","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320100213","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,13]],"date-time":"2023-11-13T03:37:04Z","timestamp":1699846624000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320100213"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1981,1]]},"references-count":12,"journal-issue":{"issue":"2","published-print":{"date-parts":[[1981,1]]}},"alternative-id":["10.1002\/ajmg.1320100213"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320100213","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1981,1]]}}}