{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:06:04Z","timestamp":1761717964653},"reference-count":10,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":3805,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Prenat. Diagn."],"published-print":{"date-parts":[[2005,4]]},"DOI":"10.1002\/pd.1105","type":"journal-article","created":{"date-parts":[[2005,4,22]],"date-time":"2005-04-22T16:17:16Z","timestamp":1114186636000},"page":"292-295","source":"Crossref","is-referenced-by-count":9,"title":["Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement"],"prefix":"10.1002","volume":"25","author":[{"given":"Ant\u00f3nio","family":"Pires","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lina","family":"Ramos","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Margarida","family":"Ven\u00e2ncio","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ana Isabel","family":"Rei","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S\u00e9rgio","family":"Castedo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jorge","family":"Saraiva","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,4,22]]},"reference":[{"issue":"1","key":"10.1002\/pd.1105-BIB1|cit1","doi-asserted-by":"crossref","first-page":"33","DOI":"10.1002\/ajmg.1320550111","article-title":"Duplication 3p syndrome: a molecular delineation of the critical region","volume":"55","author":"Aqua","year":"1995","journal-title":"Am J Med Genet"},{"issue":"1","key":"10.1002\/pd.1105-BIB2|cit2","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1002\/1097-0223(200101)21:1<73::AID-PD993>3.0.CO;2-8","article-title":"Prenatal diagnosis of partial trisomy 3q(3q22-qter) and monosomy 6q(6q25.3-qter) in a fetus with sonographic findings of cystic hygromata colli and unilateral pleural effusion","volume":"21","author":"Chen","year":"2001","journal-title":"Prenat Diagn"},{"key":"10.1002\/pd.1105-BIB3|cit3","doi-asserted-by":"crossref","first-page":"321","DOI":"10.1111\/j.1399-0004.1996.tb02382.x","article-title":"Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly","volume":"50","author":"Chen","year":"1996","journal-title":"Clin Genet"},{"issue":"1","key":"10.1002\/pd.1105-BIB4|cit4","doi-asserted-by":"crossref","first-page":"49","DOI":"10.1111\/j.1399-0004.1995.tb04054.x","article-title":"Molecular characterization of trisomic 3p24.1-3pter: a case with review of the literature","volume":"48","author":"Conte","year":"1995","journal-title":"Clin Genet"},{"issue":"1","key":"10.1002\/pd.1105-BIB5|cit5","first-page":"65","article-title":"A new case of partial trisomy 3 (q25-qter) in a newborn","volume":"31","author":"Montero","year":"1988","journal-title":"Ann Genet"},{"key":"10.1002\/pd.1105-BIB6|cit6","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1111\/j.1399-0004.1986.tb00568.x","article-title":"Partial trisomy 3p syndrome","volume":"30","author":"Reiss","year":"1986","journal-title":"Clin Genet"},{"key":"10.1002\/pd.1105-BIB7|cit7","volume-title":"Catalogue of Unbalanced Chromosome Aberrations in Man","author":"Schinzel","year":"2001"},{"key":"10.1002\/pd.1105-BIB8|cit8","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1002\/ajmg.1320100210","article-title":"The dup(3q) syndrome: Report of eight cases and review of the literature","volume":"10","author":"Steinbach","year":"1981","journal-title":"Am J Med Genet"},{"issue":"2","key":"10.1002\/pd.1105-BIB9|cit9","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1111\/j.1399-0004.1987.tb03342.x","article-title":"Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1;p23)","volume":"32","author":"Tranebjaerg","year":"1987","journal-title":"Clin Genet"},{"key":"10.1002\/pd.1105-BIB10|cit10","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1002\/ajmg.1320220113","article-title":"Further delineation of the dup(3q) syndrome","volume":"22","author":"Wilson","year":"1985","journal-title":"Am J Med Genet"}],"container-title":["Prenatal Diagnosis"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fpd.1105","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/pd.1105","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,7,3]],"date-time":"2021-07-03T22:43:32Z","timestamp":1625352212000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/pd.1105"}},"subtitle":["PRENATAL FOETAL DIAGNOSIS OF PARTIAL TRISOMY 3Q AND MONOSOMY 13P"],"short-title":[],"issued":{"date-parts":[[2005,4]]},"references-count":10,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2005,4]]}},"URL":"https:\/\/doi.org\/10.1002\/pd.1105","archive":["Portico"],"relation":{},"ISSN":["0197-3851"],"issn-type":[{"value":"0197-3851","type":"print"}],"subject":[],"published":{"date-parts":[[2005,4]]}}}