{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,15]],"date-time":"2026-10-15T14:52:25Z","timestamp":1792075945224,"version":"4.4.0"},"update-to":[{"DOI":"10.1016\/j.ejogrb.2025.114023","type":"retraction","label":"Retraction","source":"publisher","updated":{"date-parts":[[2025,7,1]],"date-time":"2025-07-01T00:00:00Z","timestamp":1751328000000}}],"reference-count":20,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2025,7,1]],"date-time":"2025-07-01T00:00:00Z","timestamp":1751328000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2025,7,1]],"date-time":"2025-07-01T00:00:00Z","timestamp":1751328000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","ejog.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["European Journal of Obstetrics &amp; Gynecology and Reproductive Biology"],"published-print":{"date-parts":[[2025,7]]},"DOI":"10.1016\/j.ejogrb.2025.114023","type":"journal-article","created":{"date-parts":[[2025,4,30]],"date-time":"2025-04-30T23:40:53Z","timestamp":1746056453000},"page":"114023","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"special_numbering":"C","title":["RETRACTED: Prenatal diagnosis and molecular cytogenetic analyses of a rare 17q12 microdeletion and 17q11.2 microduplication family with normal phenotype"],"prefix":"10.1016","volume":"311","author":[{"given":"Weihua","family":"Tian","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qi","family":"Xia","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xian","family":"He","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pei","family":"Leng","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.ejogrb.2025.114023_b0005","unstructured":"Mitchel MW, Moreno-De-Luca D, Myers SM, Levy RV, Turner S, Ledbetter DH, Martin CL. 17q12 Recurrent Deletion Syndrome. 2016 Dec 8 [updated 2020 Oct 15]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews\u00ae [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2022. PMID: 27929632."},{"key":"10.1016\/j.ejogrb.2025.114023_b0010","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1186\/s13039-019-0431-7","article-title":"Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities","volume":"12","author":"Wan","year":"2019","journal-title":"Mol Cytogenet"},{"issue":"2","key":"10.1016\/j.ejogrb.2025.114023_b0015","doi-asserted-by":"crossref","first-page":"232","DOI":"10.1016\/j.tjog.2021.01.001","article-title":"Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series","volume":"60","author":"Zhou","year":"2021","journal-title":"Taiwan J Obstet Gynecol"},{"issue":"3","key":"10.1016\/j.ejogrb.2025.114023_b0020","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1080\/01443615.2018.1519693","article-title":"Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case series","volume":"39","author":"Jing","year":"2019","journal-title":"J Obstet Gynaecol"},{"key":"10.1016\/j.ejogrb.2025.114023_b0025","doi-asserted-by":"crossref","unstructured":"Ya\u015far K\u00f6stek H, \u00d6zg\u00fc\u00e7 \u00c7\u00f6mlek F, G\u00fcrkan H, \u00d6zkay\u0131n EN, T\u00fct\u00fcnc\u00fcler K\u00f6kenli F. A Case of Diabetes Mellitus Type MODY5 as a feature of 17q12 Deletion Syndrome. J Clin Res Pediatr Endocrinol. 2022 Dec 13. doi: 10.4274\/jcrpe.galenos.2022.2022-3-2. Epub ahead of print. PMID: 36511482.","DOI":"10.4274\/jcrpe.galenos.2022.2022-3-2"},{"key":"10.1016\/j.ejogrb.2025.114023_b0030","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1186\/1750-1172-4-25","article-title":"Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports","volume":"4","author":"Bernardini","year":"2009","journal-title":"Orphanet J Rare Dis"},{"issue":"1","key":"10.1016\/j.ejogrb.2025.114023_b0035","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1097\/YPG.0000000000000302","article-title":"Co-existing bipolar disease and 17q12 deletion: a rare case report","volume":"32","author":"Bulu","year":"2022","journal-title":"Psychiatr Genet"},{"issue":"7","key":"10.1016\/j.ejogrb.2025.114023_b0040","doi-asserted-by":"crossref","first-page":"345","DOI":"10.1111\/pcn.13367","article-title":"Psychiatric patients with a de novo 17q12 deletion: Two case reports","volume":"76","author":"Kushima","year":"2022","journal-title":"Psychiatry Clin Neurosci"},{"issue":"6","key":"10.1016\/j.ejogrb.2025.114023_b0045","doi-asserted-by":"crossref","first-page":"871","DOI":"10.1016\/j.tjog.2016.08.004","article-title":"Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality","volume":"55","author":"Chen","year":"2016","journal-title":"Taiwan J Obstet Gynecol"},{"issue":"1","key":"10.1016\/j.ejogrb.2025.114023_b0050","doi-asserted-by":"crossref","DOI":"10.1016\/j.gim.2024.101227","article-title":"A systematic review and pooled analysis of penetrance estimates of copy-number variants associated with neurodevelopment","volume":"27","author":"Goh","year":"2025","journal-title":"Genet Med"},{"issue":"3","key":"10.1016\/j.ejogrb.2025.114023_b0055","doi-asserted-by":"crossref","first-page":"426","DOI":"10.1016\/j.tjog.2024.03.012","article-title":"Prenatal diagnosis of familial 17q11.2 duplication encompassing NF1 in a pregnancy associated with asymptomatic carrier parent","volume":"63","author":"Chen","year":"2024","journal-title":"Taiwan J Obstet Gynecol"},{"issue":"4","key":"10.1016\/j.ejogrb.2025.114023_b0060","doi-asserted-by":"crossref","first-page":"349","DOI":"10.24920\/004009","article-title":"Novel Pathogenic Mutation of PNPLA1 Identified in Autosomal Recessive Congenital Ichthyosis: A Case Report","volume":"37","author":"Li","year":"2022","journal-title":"Chin Med Sci J"},{"key":"10.1016\/j.ejogrb.2025.114023_b0065","doi-asserted-by":"crossref","unstructured":"Zeng F, Qin W, Huang F, Chang P. PNPLA1-Mediated Acylceramide Biosynthesis and Autosomal Recessive Congenital Ichthyosis. Metabolites. 2022;12(8):685. Published 2022 Jul 26. doi:10.3390\/metabo12080685.","DOI":"10.3390\/metabo12080685"},{"key":"10.1016\/j.ejogrb.2025.114023_b0070","doi-asserted-by":"crossref","unstructured":"Bai W, Zhang Q, Lin Z, et al. Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing. Front Endocrinol (Lausanne). 2023;14:1218793. Published 2023 Oct 17. doi:10.3389\/fendo.2023.1218793.","DOI":"10.3389\/fendo.2023.1218793"},{"key":"10.1016\/j.ejogrb.2025.114023_b0075","doi-asserted-by":"crossref","unstructured":"Luo M, Gu X, Zhou T, Chen C. Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene. Mol Cytogenet. 2022;15(1):53. Published 2022 Dec 21. doi:10.1186\/s13039-022-00632-y.","DOI":"10.1186\/s13039-022-00632-y"},{"issue":"3","key":"10.1016\/j.ejogrb.2025.114023_b0080","doi-asserted-by":"crossref","first-page":"348","DOI":"10.1007\/s10930-021-09991-8","article-title":"A Review of Functional Characterization of Single Amino Acid Change Mutations in HNF Transcription Factors in MODY Pathogenesis","volume":"40","author":"\u00c7ubuk","year":"2021","journal-title":"Protein J"},{"issue":"4","key":"10.1016\/j.ejogrb.2025.114023_b0085","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0018858","article-title":"Lhx1 is required for specification of the renal progenitor cell field","volume":"6","author":"Cirio","year":"2011","journal-title":"PLoS One"},{"issue":"6","key":"10.1016\/j.ejogrb.2025.114023_b0090","doi-asserted-by":"crossref","first-page":"478","DOI":"10.1038\/gim.2012.164","article-title":"Estimates of penetrance for recurrent pathogenic copy-number variations","volume":"15","author":"Rosenfeld","year":"2013","journal-title":"Genet Med"},{"issue":"4","key":"10.1016\/j.ejogrb.2025.114023_b0095","doi-asserted-by":"crossref","first-page":"224","DOI":"10.1038\/nrg.2015.25","article-title":"Mechanisms underlying structural variant formation in genomic disorders","volume":"17","author":"Carvalho","year":"2016","journal-title":"Nat Rev Genet"},{"key":"10.1016\/j.ejogrb.2025.114023_b0100","article-title":"Mechanisms of structural chromosomal rearrangement formation","volume":"15(1):23","author":"Burssed","year":"2022","journal-title":"Mol Cytogenet"}],"updated-by":[{"DOI":"10.1016\/j.ejogrb.2025.114023","type":"retraction","label":"Retraction","source":"publisher","updated":{"date-parts":[[2025,7,1]],"date-time":"2025-07-01T00:00:00Z","timestamp":1751328000000}},{"DOI":"10.1016\/j.ejogrb.2026.115027","type":"erratum","label":"Erratum","source":"publisher","updated":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T00:00:00Z","timestamp":1777593600000}}],"container-title":["European Journal of Obstetrics &amp; Gynecology and Reproductive Biology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0301211525002994?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0301211525002994?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2026,3,31]],"date-time":"2026-03-31T03:43:58Z","timestamp":1774928638000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0301211525002994"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,7]]},"references-count":20,"alternative-id":["S0301211525002994"],"URL":"https:\/\/doi.org\/10.1016\/j.ejogrb.2025.114023","relation":{},"ISSN":["0301-2115"],"issn-type":[{"value":"0301-2115","type":"print"}],"subject":[],"published":{"date-parts":[[2025,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"RETRACTED: Prenatal diagnosis and molecular cytogenetic analyses of a rare 17q12 microdeletion and 17q11.2 microduplication family with normal phenotype","name":"articletitle","label":"Article Title"},{"value":"European Journal of Obstetrics & Gynecology and Reproductive Biology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejogrb.2025.114023","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2025 Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.","name":"copyright","label":"Copyright"}],"article-number":"114023"}}