{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,20]],"date-time":"2026-09-20T01:35:32Z","timestamp":1789868132599,"version":"4.0.1"},"reference-count":31,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2021,3,1]],"date-time":"2021-03-01T00:00:00Z","timestamp":1614556800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2020,12,16]],"date-time":"2020-12-16T00:00:00Z","timestamp":1608076800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["fertstertreports.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["F&amp;S Reports"],"published-print":{"date-parts":[[2021,3]]},"DOI":"10.1016\/j.xfre.2020.12.003","type":"journal-article","created":{"date-parts":[[2020,12,25]],"date-time":"2020-12-25T00:02:36Z","timestamp":1608854556000},"page":"72-79","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":3,"title":["Criteria to evaluate patterns of segmental and complete aneuploidies in preimplantation genetic testing for aneuploidy results suggestive of an inherited balanced translocation or inversion"],"prefix":"10.1016","volume":"2","author":[{"given":"Alyssa C.","family":"Snider","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5661-4974","authenticated-orcid":false,"given":"Tristan","family":"Darvin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lauren","family":"Spor","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adedoyin","family":"Akinwole","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cengiz","family":"Cinnioglu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Refik","family":"Kayali","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.xfre.2020.12.003_bib1","first-page":"995","article-title":"De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints","volume":"49","author":"Warburton","year":"1991","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib2","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1002\/pd.1970040706","article-title":"Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis","volume":"4","author":"Warburton","year":"1984","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.xfre.2020.12.003_bib3","series-title":"Chromosome translocation","first-page":"1","article-title":"Historical and clinical perspectives on chromosomal translocations","author":"Wilch","year":"2018"},{"key":"10.1016\/j.xfre.2020.12.003_bib4","first-page":"136","article-title":"Mental retardation qssociated with \u201cbalanced\u201d chromosome rearrangements","volume":"29","author":"Funderburk","year":"1977","journal-title":"Am J Hum Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib5","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1111\/j.1399-0004.1975.tb01498.x","article-title":"A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities","volume":"8","author":"Hamerton","year":"1975","journal-title":"Clin Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib6","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1080\/09723757.2012.11886186","article-title":"A retrospective study of balanced chromosomal translocations in a Turkish population","volume":"12","author":"Karakus","year":"2012","journal-title":"Int J Hum Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib7","series-title":"The principles of clinical cytogenetics","year":"2013"},{"key":"10.1016\/j.xfre.2020.12.003_bib8","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1007\/BF00292366","article-title":"The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families","volume":"64","author":"Iselius","year":"1983","journal-title":"Hum Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib9","doi-asserted-by":"crossref","first-page":"1437","DOI":"10.1002\/(SICI)1097-0223(199812)18:13<1437::AID-PD497>3.0.CO;2-P","article-title":"Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis","volume":"18","author":"Scriven","year":"1998","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.xfre.2020.12.003_bib10","doi-asserted-by":"crossref","first-page":"1037","DOI":"10.1016\/j.fertnstert.2014.12.118","article-title":"Pregnancy outcomes following 24-chromosome preimplantation genetic diagnosis in couples with balanced reciprocal or Robertsonian translocations","volume":"103","author":"Idowu","year":"2015","journal-title":"Fertil Steril"},{"key":"10.1016\/j.xfre.2020.12.003_bib11","doi-asserted-by":"crossref","first-page":"760","DOI":"10.1016\/j.rbmo.2015.09.002","article-title":"Validation of next-generation sequencing for comprehensive chromosome screening of embryos","volume":"31","author":"Kung","year":"2015","journal-title":"Reprod Biomed Online"},{"key":"10.1016\/j.xfre.2020.12.003_bib12","doi-asserted-by":"crossref","first-page":"1566","DOI":"10.1093\/humrep\/dey227","article-title":"Defining the limits of detection for chromosome rearrangements in the preimplantation embryo using next generation sequencing","volume":"33","author":"Cuman","year":"2018","journal-title":"Hum Reprod"},{"key":"10.1016\/j.xfre.2020.12.003_bib13","doi-asserted-by":"crossref","first-page":"1818","DOI":"10.1093\/humrep\/deq101","article-title":"Predictive value of sperm-FISH analysis on the outcome of preimplantation genetic diagnosis (PGD) for a pericentric inversion inv5(p15.3q11.2) carrier","volume":"25","author":"Bernicot","year":"2010","journal-title":"Hum Reprod"},{"key":"10.1016\/j.xfre.2020.12.003_bib14","doi-asserted-by":"crossref","first-page":"760","DOI":"10.1002\/pd.171","article-title":"Preimplantation genetic diagnosis of pericentric inversions","volume":"21","author":"Escudero","year":"2001","journal-title":"Prenat Diagn"},{"key":"10.1016\/j.xfre.2020.12.003_bib15","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1136\/jmg.29.2.103","article-title":"Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding","volume":"29","author":"Jacobs","year":"1992","journal-title":"J Med Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib16","doi-asserted-by":"crossref","first-page":"800","DOI":"10.1016\/j.fertnstert.2007.04.032","article-title":"Genetic screening in 2,710 infertile candidate couples for assisted reproductive techniques: results of application of Italian guidelines for the appropriate use of genetic tests","volume":"89","author":"Riccaboni","year":"2008","journal-title":"Fertil Steril"},{"key":"10.1016\/j.xfre.2020.12.003_bib17","series-title":"Gardner and Sutherland\u2019s chromosome abnormalities and genetic counseling","author":"Gardner","year":"2018"},{"key":"10.1016\/j.xfre.2020.12.003_bib18","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1007\/BF01876812","article-title":"A cytogenetic survey of 14,835 consecutive liveborns","volume":"36","author":"Maeda","year":"1991","journal-title":"Jinrui Idengaku Zasshi"},{"key":"10.1016\/j.xfre.2020.12.003_bib19","doi-asserted-by":"crossref","first-page":"519","DOI":"10.1093\/oxfordjournals.humrep.a137135","article-title":"Cytogenetic studies in couples experiencing repeated pregnancy losses","volume":"5","author":"De Braekeleer","year":"1990","journal-title":"Hum Reprod"},{"key":"10.1016\/j.xfre.2020.12.003_bib20","doi-asserted-by":"crossref","first-page":"1103","DOI":"10.1016\/j.fertnstert.2012.06.048","article-title":"Evaluation and treatment of recurrent pregnancy loss: a committee opinion","volume":"98","year":"2012","journal-title":"Fertil Steril"},{"key":"10.1016\/j.xfre.2020.12.003_bib21","doi-asserted-by":"crossref","first-page":"899","DOI":"10.1111\/j.1471-0528.1985.tb03069.x","article-title":"Recurrent pregnancy losses and parental chromosome abnormalities: a review","volume":"92","author":"Tharapel","year":"1985","journal-title":"Br J Obstet Gynaecol"},{"key":"10.1016\/j.xfre.2020.12.003_bib22","doi-asserted-by":"crossref","first-page":"2549","DOI":"10.1093\/humrep\/dex324","article-title":"The incidence and origin of segmental aneuploidy in human oocytes and preimplantation embryos","volume":"32","author":"Babariya","year":"2017","journal-title":"Hum Reprod"},{"key":"10.1016\/j.xfre.2020.12.003_bib23","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1186\/s13039-019-0423-7","article-title":"Analysis of meiotic segregation modes in biopsied blastocysts from preimplantation genetic testing cycles of reciprocal translocations","volume":"12","author":"Wang","year":"2019","journal-title":"Mol Cytogenet"},{"key":"10.1016\/j.xfre.2020.12.003_bib24","doi-asserted-by":"crossref","first-page":"2144","DOI":"10.1016\/j.fertnstert.2007.10.035","article-title":"Estimation of chromosomal imbalances in preimplantation embryos from preimplantation genetic diagnosis cycles of reciprocal translocations with or without acrocentric chromosomes","volume":"90","author":"Lim","year":"2008","journal-title":"Fertil Steril"},{"key":"10.1016\/j.xfre.2020.12.003_bib25","doi-asserted-by":"crossref","first-page":"1369","DOI":"10.1016\/j.fertnstert.2012.12.010","article-title":"Preimplantation genetic diagnosis outcomes and meiotic segregation\u00a0analysis of robertsonian translocation carriers","volume":"99","author":"Sung Ko","year":"2013","journal-title":"Fertil Steril"},{"key":"10.1016\/j.xfre.2020.12.003_bib26","doi-asserted-by":"crossref","first-page":"46046","DOI":"10.1371\/journal.pone.0046046","article-title":"Chromosome segregation analysis in human embryos obtained from couples involving male carriers of reciprocal or Robertsonian translocation","volume":"7","author":"Yilmaz","year":"2012","journal-title":"PLoS One"},{"key":"10.1016\/j.xfre.2020.12.003_bib27","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/j.rbmo.2011.08.012","article-title":"Meiotic segregation analysis of embryos from reciprocal translocation carriers in PGD cycles","volume":"24","author":"Ye","year":"2012","journal-title":"Reprod Biomed Online"},{"key":"10.1016\/j.xfre.2020.12.003_bib28","doi-asserted-by":"crossref","first-page":"1483","DOI":"10.1007\/s10815-017-1009-0","article-title":"Natural selection between day 3 and day 5\/6 PGD embryos in couples with reciprocal or Robertsonian translocations","volume":"34","author":"Beyer","year":"2017","journal-title":"J Assist Reprod Genet"},{"key":"10.1016\/j.xfre.2020.12.003_bib29","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1159\/000086904","article-title":"Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes","volume":"111","author":"Munn\u00e9","year":"2005","journal-title":"Cytogenet Genome Res"},{"key":"10.1016\/j.xfre.2020.12.003_bib30","doi-asserted-by":"crossref","first-page":"2581","DOI":"10.1093\/humrep\/det271","article-title":"Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers","volume":"28","author":"Tan","year":"2013","journal-title":"Hum Reprod"},{"key":"10.1016\/j.xfre.2020.12.003_bib31","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1159\/000132023","article-title":"Pachytene analysis of a man with a 13q;14q translocation and infertility","volume":"38","author":"Luciani","year":"1984","journal-title":"Cytogenet Genome Res"}],"container-title":["F&amp;S Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S266633412030129X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S266633412030129X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T21:04:45Z","timestamp":1762981485000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S266633412030129X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,3]]},"references-count":31,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2021,3]]}},"alternative-id":["S266633412030129X"],"URL":"https:\/\/doi.org\/10.1016\/j.xfre.2020.12.003","relation":{},"ISSN":["2666-3341"],"issn-type":[{"value":"2666-3341","type":"print"}],"subject":[],"published":{"date-parts":[[2021,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Criteria to evaluate patterns of segmental and complete aneuploidies in preimplantation genetic testing for aneuploidy results suggestive of an inherited balanced translocation or inversion","name":"articletitle","label":"Article Title"},{"value":"F&S Reports","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.xfre.2020.12.003","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 The Author(s). Published by Elsevier Inc. on behalf of American Society for Reproductive Medicine.","name":"copyright","label":"Copyright"}]}}