{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T08:06:04Z","timestamp":1790064364555,"version":"4.0.1"},"reference-count":18,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2005,11,21]],"date-time":"2005-11-21T00:00:00Z","timestamp":1132531200000},"content-version":"vor","delay-in-days":4403,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[1993,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>We report on the prenatal diagnosis of congenital myotonic dystrophy in a case of nonimmune hydrops fetalis. DNA analysis of amniocytes revealed expansion of the trinucleotide (CTG) repeat within the myotonin PK gene, associated with myotonic dystrophy. The fetus was found to have approximately 1730 copies, while the normal population has between 5 and 27 copies, and minimally affected individuals have at least 50 copies.<\/jats:p>","DOI":"10.1002\/pd.1970131104","type":"journal-article","created":{"date-parts":[[2007,3,4]],"date-time":"2007-03-04T06:41:20Z","timestamp":1172990480000},"page":"1027-1030","source":"Crossref","is-referenced-by-count":20,"title":["DNA confirmation of congenital myotonic dystrophy in non\u2010immune hydrops fetalis"],"prefix":"10.1002","volume":"13","author":[{"given":"Robert F.","family":"Stratton","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert M.","family":"Patterson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2005,11,21]]},"reference":[{"key":"e_1_2_1_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9378(92)91365-H"},{"key":"e_1_2_1_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/0092-8674(92)90154-5"},{"key":"e_1_2_1_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-3476(88)80651-6"},{"key":"e_1_2_1_5_1","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1111\/j.1742-1241.1967.tb07117.x","article-title":"Myotonic dystrophy: its occurrence in childhood","volume":"21","author":"Gordon N.","year":"1967","journal-title":"Br. J. Clin. Pract."},{"key":"e_1_2_1_6_1","first-page":"347","article-title":"Nonimmunologic hydrops fetalis: a review of 61 cases","volume":"59","author":"Hutchinson A. A.","year":"1982","journal-title":"Obstet. Gynecol."},{"key":"e_1_2_1_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9378(84)90749-X"},{"key":"e_1_2_1_8_1","first-page":"568","article-title":"Nonimmune hydrops fetalis associated with genetic abnormalities","volume":"75","author":"Jauniaux E.","year":"1990","journal-title":"Obstet. Gynecol."},{"key":"e_1_2_1_9_1","first-page":"1867","article-title":"La maladie de Steinert n\u00e9onatal","volume":"46","author":"L'Hirondel J.","year":"1970","journal-title":"Sem. H\u01d2p. Paris"},{"key":"e_1_2_1_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1471-0528.1970.tb03511.x"},{"key":"e_1_2_1_11_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320340313"},{"key":"e_1_2_1_12_1","first-page":"571","article-title":"Prenatal diagnosis and management of nonimmunologic hydrops fetalis","volume":"56","author":"Maidman J. E.","year":"1980","journal-title":"Obstet. Gynecol"},{"key":"e_1_2_1_13_1","first-page":"263","article-title":"Forme n\u00e9onatale de la maladie de Steinert","volume":"27","author":"Messer J.","year":"1973","journal-title":"Ada Pediatr. Belg."},{"key":"e_1_2_1_14_1","doi-asserted-by":"publisher","DOI":"10.1136\/adc.54.5.331"},{"key":"e_1_2_1_15_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0002-9378(16)40458-8"},{"key":"e_1_2_1_16_1","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1976.00500070001001"},{"key":"e_1_2_1_17_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0046-8177(84)80312-3"},{"key":"e_1_2_1_18_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0095-5108(18)31015-7"},{"key":"e_1_2_1_19_1","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1542\/peds.89.1.81","article-title":"Genetic causes of hydrops fetalis","volume":"89","author":"Van Maldergem L.","year":"1992","journal-title":"Pediatrics"}],"container-title":["Prenatal Diagnosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fpd.1970131104","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/pd.1970131104","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,25]],"date-time":"2023-10-25T01:49:05Z","timestamp":1698198545000},"score":1,"resource":{"primary":{"URL":"https:\/\/obgyn.onlinelibrary.wiley.com\/doi\/10.1002\/pd.1970131104"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1993,11]]},"references-count":18,"journal-issue":{"issue":"11","published-print":{"date-parts":[[1993,11]]}},"alternative-id":["10.1002\/pd.1970131104"],"URL":"https:\/\/doi.org\/10.1002\/pd.1970131104","archive":["Portico"],"relation":{},"ISSN":["0197-3851","1097-0223"],"issn-type":[{"value":"0197-3851","type":"print"},{"value":"1097-0223","type":"electronic"}],"subject":[],"published":{"date-parts":[[1993,11]]}}}