{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,18]],"date-time":"2026-10-18T02:10:33Z","timestamp":1792289433208,"version":"4.4.0"},"reference-count":12,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2005,6,3]],"date-time":"2005-06-03T00:00:00Z","timestamp":1117756800000},"content-version":"vor","delay-in-days":9285,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Am. J. Med. Genet."],"published-print":{"date-parts":[[1980,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A survey of the birth prevalence of congenital anomalies among newborn infants in Japan is under way at a large maternity hospital in Tokyo. Of 14,430 consecutive newborn babies (7,455 M; 6,975 F), 33 had a multiple congenital anomalies (MCA) syndrome. These included 2 with trisomy 13 (including a mosaic), 3 with trisomy 18 (including 1 mosaic), 16 with trisomy 21 (including 1 mosaic), 1 with cri\u2010du\u2010chat syndrome, 1 with 5p partial trisomy, 1 with Hallermann\u2010Streiff syndrome, 1 with Treacher\u2010Collins syndrome, 1 with achondroplasia, 2 with arthrogryposis multiplex congenita, 1 with hemihypertrophy, 1 with Wiedemann\u2010Beckwith syndrome, 1 with asplenia syndrome, 1 with Klippel\u2010Trenaunay\u2010Weber syndrome, and 1 with probable Marfan's syndrome. Except for one infant with Ullrich\u2010Turner syndrome, cases with sex\u2010chromosome aberrations could not be diagnosed neonatally on a clinical basis.<\/jats:p>","DOI":"10.1002\/ajmg.1320060303","type":"journal-article","created":{"date-parts":[[2005,6,11]],"date-time":"2005-06-11T17:35:55Z","timestamp":1118511355000},"page":"189-194","source":"Crossref","is-referenced-by-count":34,"title":["The birth prevalence of malformation syndromes in Tokyo infants: A survey of 14,430 newborn infants"],"prefix":"10.1002","volume":"6","author":[{"given":"Makoto","family":"Higurashi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kumiko","family":"Iijima","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y\u00f4ko","family":"Sugimoto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Norihiko","family":"Ishikawa","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hiroki","family":"Hoshina","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nobuo","family":"Watanabe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kuniyoshi","family":"Yoneyama","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"James R.","family":"Miller","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John M.","family":"Opitz","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,6,3]]},"reference":[{"key":"e_1_2_1_2_2","first-page":"160","volume-title":"Clinical Atlas of Human Chromosomes","author":"De Grouchy J","year":"1977"},{"key":"e_1_2_1_3_2","first-page":"129","article-title":"Gestational ages and intrauterine growth","volume":"4","author":"Funakawa H","year":"1968","journal-title":"Acta Neonatol Jpn"},{"key":"e_1_2_1_4_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1399-0004.1975.tb01498.x"},{"key":"e_1_2_1_5_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1651-2227.1977.tb07934.x"},{"key":"e_1_2_1_6_2","first-page":"333","article-title":"A case with Hallermann Streif syndrome","volume":"36","author":"Hoshina H","year":"1973","journal-title":"J Pediatr Pract"},{"key":"e_1_2_1_7_2","first-page":"44","article-title":"Dermatoglyphic study of Down's syndrome in Japan","volume":"13","author":"Matsui I","year":"1966","journal-title":"Paediatr Univ Tokyo"},{"key":"e_1_2_1_8_2","first-page":"131","article-title":"Chromosomal abberations","volume":"36","author":"Matsui I","year":"1969","journal-title":"Obstet Gynecol"},{"key":"e_1_2_1_9_2","doi-asserted-by":"publisher","DOI":"10.1016\/0014-4827(60)90138-5"},{"key":"e_1_2_1_10_2","first-page":"125","volume-title":"Medical Genetics","author":"Nora JJ","year":"1974"},{"key":"e_1_2_1_11_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(71)90287-X"},{"key":"e_1_2_1_12_2","doi-asserted-by":"publisher","DOI":"10.1002\/9780470720097.ch8"},{"key":"e_1_2_1_13_2","doi-asserted-by":"publisher","DOI":"10.1136\/adc.30.151.257"}],"container-title":["American Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fajmg.1320060303","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.1320060303","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,11,13]],"date-time":"2023-11-13T00:15:19Z","timestamp":1699834519000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.1320060303"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1980,1]]},"references-count":12,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1980,1]]}},"alternative-id":["10.1002\/ajmg.1320060303"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.1320060303","archive":["Portico"],"relation":{},"ISSN":["0148-7299","1096-8628"],"issn-type":[{"value":"0148-7299","type":"print"},{"value":"1096-8628","type":"electronic"}],"subject":[],"published":{"date-parts":[[1980,1]]}}}