{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,27]],"date-time":"2026-06-27T02:56:04Z","timestamp":1782528964176,"version":"3.54.5"},"reference-count":23,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2024,7,1]],"date-time":"2024-07-01T00:00:00Z","timestamp":1719792000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2024,5,26]],"date-time":"2024-05-26T00:00:00Z","timestamp":1716681600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/100020595","name":"National Science and Technology Council","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100020595","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.es","clinicalkey.com.au","clinicalkey.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"published-print":{"date-parts":[[2024,7]]},"DOI":"10.1016\/j.tjog.2024.05.010","type":"journal-article","created":{"date-parts":[[2024,7,12]],"date-time":"2024-07-12T20:15:25Z","timestamp":1720815325000},"page":"561-564","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"title":["Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations"],"prefix":"10.1016","volume":"63","author":[{"given":"Chih-Ping","family":"Chen","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Fang-Tzu","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yen-Ting","family":"Pan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peih-Shan","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Meng-Shan","family":"Lee","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wayseen","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.tjog.2024.05.010_bib1","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1002\/(SICI)1097-0223(199603)16:3<270::AID-PD836>3.0.CO;2-0","article-title":"Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of long bones and a single umbilical artery","volume":"16","author":"Chen","year":"1996","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.tjog.2024.05.010_bib2","first-page":"405","article-title":"Partial monosomy 3p (3p26.2\u2192pter) and partial trisomy 5q (5q34\u2192qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay","volume":"23","author":"Chen","year":"2012","journal-title":"Genet Counsel"},{"key":"10.1016\/j.tjog.2024.05.010_bib3","doi-asserted-by":"crossref","first-page":"435","DOI":"10.1016\/j.tjog.2012.07.022","article-title":"Pure partial monosomy 3p (3p25.3\u2192pter): prenatal diagnosis and array comparative genomic hybridization characterization","volume":"51","author":"Chen","year":"2012","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2024.05.010_bib4","doi-asserted-by":"crossref","first-page":"278","DOI":"10.1016\/j.tjog.2013.04.023","article-title":"Prenatal diagnosis of distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization","volume":"52","author":"Chen","year":"2013","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2024.05.010_bib5","doi-asserted-by":"crossref","first-page":"288","DOI":"10.1016\/j.tjog.2016.02.015","article-title":"Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3\u2192pter) and partial trisomy 16q (16q23.1\u2192qter)","volume":"55","author":"Chen","year":"2016","journal-title":"Taiwan J Obstet Gynecol"},{"key":"10.1016\/j.tjog.2024.05.010_bib6","doi-asserted-by":"crossref","first-page":"2099","DOI":"10.1002\/ajmg.a.32824","article-title":"Microarray based analysis of 3p25-p26 deletions (3p- syndrome)","volume":"149A","author":"Shuib","year":"2009","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib7","doi-asserted-by":"crossref","first-page":"11754","DOI":"10.1073\/pnas.162241099","article-title":"The novel Rho-GTPase activating gene MEGAP\/srGAP3 has a putative role in severe mental retardation","volume":"99","author":"Endris","year":"2002","journal-title":"Proc Nat Acad Sci USA"},{"key":"10.1016\/j.tjog.2024.05.010_bib8","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1016\/j.ajhg.2016.11.010","article-title":"Mutations in histone acetylase modifier BRPF1 cause an autosomal-dominant form of intellectual disability with associated ptosis","volume":"100","author":"Mattioli","year":"2017","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib9","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1016\/j.ajhg.2016.11.011","article-title":"Mutations in the chromatin regulator gene BRPF1 cause syndromic intellectual disability and deficient histone acetylation","volume":"100","author":"Yan","year":"2017","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib10","doi-asserted-by":"crossref","first-page":"1674","DOI":"10.1016\/S0140-6736(12)61480-9","article-title":"Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study","volume":"380","author":"Rauch","year":"2012","journal-title":"Lancet"},{"key":"10.1016\/j.tjog.2024.05.010_bib11","doi-asserted-by":"crossref","first-page":"618","DOI":"10.1016\/j.ajhg.2014.03.006","article-title":"De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability","volume":"94","author":"Grozeva","year":"2014","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib12","doi-asserted-by":"crossref","first-page":"753","DOI":"10.1038\/ejhg.2014.165","article-title":"Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome","volume":"23","author":"Kuechler","year":"2015","journal-title":"Eur J Hum Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib13","doi-asserted-by":"crossref","first-page":"994","DOI":"10.1136\/jmg.32.12.994","article-title":"Del(3)(p25.3) without phenotypic effect","volume":"32","author":"Knight","year":"1995","journal-title":"J\u00a0Med Genet"},{"issue":"Suppl","key":"10.1016\/j.tjog.2024.05.010_bib14","first-page":"301","article-title":"Deletion 3p25.3 in a mother and daughter with normal phenotype","volume":"71","author":"Jervis","year":"2002","journal-title":"Am J Hum Genet"},{"issue":"Suppl","key":"10.1016\/j.tjog.2024.05.010_bib15","first-page":"301","article-title":"Deletion 3p25 in a mother and child","volume":"71","author":"Sklower-Brooks","year":"2002","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib16","first-page":"401","article-title":"Follow-up of an intelligent odd-mannered teenager with del(3)(p26). Remarks on authorship and ethical commitment","volume":"17","author":"Rivera","year":"2006","journal-title":"Genet Counsel"},{"key":"10.1016\/j.tjog.2024.05.010_bib17","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1002\/ajmg.a.31066","article-title":"Karyotype-phenotype analysis and molecular delineation of a 3p26 deletion\/8q24.3 duplication case with a virtually normal phenotype and mild cognitive deficit","volume":"140A","author":"Shrimpton","year":"2006","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib18","doi-asserted-by":"crossref","first-page":"1587","DOI":"10.1002\/ajmg.a.31325","article-title":"Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect","volume":"140A","author":"Takagishi","year":"2006","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib19","doi-asserted-by":"crossref","first-page":"2143","DOI":"10.1002\/ajmg.a.31902","article-title":"Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review","volume":"143A","author":"Malmgren","year":"2007","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib20","doi-asserted-by":"crossref","first-page":"1899","DOI":"10.1002\/ajmg.a.32387","article-title":"Terminal 3p deletions: phenotypic variability, chromosomal non-penetrance, or gene modification?","volume":"146A","author":"Barber","year":"2008","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib21","doi-asserted-by":"crossref","first-page":"538","DOI":"10.1002\/ajmg.a.32158","article-title":"Distal 3p deletion is not necessarily associated with dysmorphic features or psychomotor delay","volume":"146A","author":"Hoo","year":"2008","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib22","doi-asserted-by":"crossref","first-page":"1059","DOI":"10.1002\/ajmg.a.33149","article-title":"3p Deletion and (skewed) literature review","volume":"152A","author":"Rivera","year":"2010","journal-title":"Am J Med Genet"},{"key":"10.1016\/j.tjog.2024.05.010_bib23","doi-asserted-by":"crossref","first-page":"2863","DOI":"10.1002\/ajmg.a.36700","article-title":"A\u00a0terminal 3p26.3 deletion is not associated with dysmorphic features and intellectual disability in a four-generation family","volume":"164A","author":"Moghadasi","year":"2014","journal-title":"Am J Med Genet"}],"container-title":["Taiwanese Journal of Obstetrics and Gynecology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455924001372?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1028455924001372?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,7,12]],"date-time":"2024-07-12T20:15:38Z","timestamp":1720815338000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1028455924001372"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,7]]},"references-count":23,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2024,7]]}},"alternative-id":["S1028455924001372"],"URL":"https:\/\/doi.org\/10.1016\/j.tjog.2024.05.010","relation":{},"ISSN":["1028-4559"],"issn-type":[{"value":"1028-4559","type":"print"}],"subject":[],"published":{"date-parts":[[2024,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations","name":"articletitle","label":"Article Title"},{"value":"Taiwanese Journal of Obstetrics and Gynecology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.tjog.2024.05.010","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2024 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}