{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,7,16]],"date-time":"2024-07-16T00:58:22Z","timestamp":1721091502322},"reference-count":16,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2005,6,2]],"date-time":"2005-06-02T00:00:00Z","timestamp":1117670400000},"content-version":"vor","delay-in-days":8219,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1982,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Ullrich\u2010Turner syndrome occurred in one of a pair of female twins. The chromosome constitution of the affected twin was 45,X\/46,XX and that of the normal twin 46,XX. Investigation of banded chromosomes, red cell antigens, HLA types, red cell enzymes, and serum proteins indicates monozygosity. The twins are discordant for height, pterygium colli, ovarian function, strabismus, dental eruption, external ear formation, hearing loss, and performance scores on the Wechsler Intelligence Test. All of these differences can be attributed to X monosomy in one cell line in the affected twin, presumably resulting from mitotic nondisjunction or anaphase lag early during embryonic development. Ten other pairs of apparently monozygotic twins discordant for the Ullrich\u2010Turner syndrome have been reported previously, and the findings in these cases are reviewed.<\/jats:p>","DOI":"10.1002\/ajmg.1320130407","type":"journal-article","created":{"date-parts":[[2005,6,12]],"date-time":"2005-06-12T00:45:33Z","timestamp":1118537133000},"page":"389-399","source":"Crossref","is-referenced-by-count":11,"title":["Monozygotic twins discordant for Ullrich\u2010Turner syndrome"],"prefix":"10.1002","volume":"13","author":[{"given":"Edra","family":"Weiss","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hannelore","family":"Loevy","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antoinette","family":"Saunders","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Samuel","family":"Pruzansky","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ira M.","family":"Rosenthal","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"John M.","family":"Opitz","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","first-page":"3","article-title":"Chromosomally discordant monozygotic twins","volume":"15","author":"Benirschke K","year":"1965","journal-title":"Hum Chromosome Newslett"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320050112"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.3.2.117"},{"key":"e_1_2_1_5_1","first-page":"91","article-title":"Time of eruption of the permanent teeth cephalometric and tooth measurement and sulphation factor activity in 45 patients with Turner's syndrome with different types of X chromosome aberrations","volume":"48","author":"Fillipsson R","year":"1965","journal-title":"Acta Endocrinol"},{"key":"e_1_2_1_6_1","first-page":"335","volume-title":"Chromosome Aberrations in Ophthalmology","author":"Fran\u00e7ois J","year":"1975"},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF01066000"},{"key":"e_1_2_1_8_1","doi-asserted-by":"publisher","DOI":"10.1177\/00220345650440012201"},{"key":"e_1_2_1_9_1","volume-title":"Bender Gestalt for Young Children","author":"Kappitz E","year":"1963"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.12.1.70"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1159\/000129770"},{"key":"e_1_2_1_12_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF01067370"},{"key":"e_1_2_1_13_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1972.tb15867.x"},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1210\/jcem-29-4-440"},{"key":"e_1_2_1_15_1","doi-asserted-by":"publisher","DOI":"10.1177\/028418517601705B03"},{"key":"e_1_2_1_16_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.3.2.124"},{"key":"e_1_2_1_17_1","first-page":"2945","article-title":"Presumption de monozygotisme en d\u00e9pit d'un dimorphisme sexual: Sujet masculin XY et sujet neutre haplo X","volume":"252","author":"Turpin R","year":"1961","journal-title":"CR Hebd Seane Acad Sci Paris"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320130407","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320130407","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,13]],"date-time":"2023-11-13T00:02:58Z","timestamp":1699833778000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320130407"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1982,12]]},"references-count":16,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1982,12]]}},"alternative-id":["10.1002\/ajmg.1320130407"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320130407","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1982,12]]}}}