Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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Material Type: Article
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Sex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXXEndocrine Connections, 2023-08, Vol.12 (9), p.1-10 [Peer Reviewed Journal]the author(s) ;the author(s) 2023 the author(s) ;ISSN: 2049-3614 ;EISSN: 2049-3614 ;DOI: 10.1530/EC-22-0440 ;PMID: 37399523Full text available |
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Peer Reviewed Journal]2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1279 ;PMID: 32463164Full text available |
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A review of trisomy X (47,XXX)Orphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Peer Reviewed Journal]COPYRIGHT 2010 BioMed Central Ltd. ;COPYRIGHT 2010 BioMed Central Ltd. ;Copyright ©2010 Tartaglia et al; licensee BioMed Central Ltd. 2010 Tartaglia et al; licensee BioMed Central Ltd. ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/1750-1172-5-8 ;PMID: 20459843Full text available |
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Material Type: Article
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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndromeJournal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Peer Reviewed Journal]Copyright 2002 Journal of Medical Genetics ;2002 INIST-CNRS ;COPYRIGHT 2002 BMJ Publishing Group Ltd. ;Copyright: 2002 Copyright 2002 Journal of Medical Genetics ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.39.3.217 ;PMID: 11897829 ;CODEN: JMDGAEFull text available |
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Material Type: Article
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Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXXGenes, 2021-06, Vol.12 (6), p.798 [Peer Reviewed Journal]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12060798 ;PMID: 34073864Full text available |
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Material Type: Article
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Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literatureMolecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00732-n/a [Peer Reviewed Journal]2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;Copyright John Wiley & Sons, Inc. Jul 2019 ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.732 ;PMID: 31070017Full text available |
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Material Type: Article
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69, XXX Karyotype Triploidy SyndromeJournal of the Turkish German Gynecological Association, 2016-05, Vol.17, p.S329 [Peer Reviewed Journal]Copyright Aves Yayincilik Ltd. STI. May 2016 ;ISSN: 1309-0399 ;EISSN: 1309-0380Full text available |
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Material Type: Article
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Premature ovarian failure related to trisomy X: Two case reports with an aberrant 47, XXX karyotypeJournal of human reproductive sciences, 2021-01, Vol.14 (1), p.87-90 [Peer Reviewed Journal]COPYRIGHT 2021 Indian Society of Assisted Reproduction ;COPYRIGHT 2021 Medknow Publications and Media Pvt. Ltd. ;2021. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright: © 2021 Journal of Human Reproductive Sciences 2021 ;ISSN: 0974-1208 ;EISSN: 1998-4766 ;DOI: 10.4103/jhrs.JHRS_59_20 ;PMID: 34083998Full text available |
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Material Type: Article
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovariesClinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Peer Reviewed Journal]2019 The Authors. published by John Wiley & Sons Ltd. ;2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.2207 ;PMID: 31183102Full text available |
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Material Type: Article
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Everyday executive functions in Down syndrome from early childhood to young adulthood: evidence for both unique and shared characteristics compared to youth with sex chromosome trisomy (XXX and XXY)Frontiers in behavioral neuroscience, 2015-10, Vol.9, p.264-264 [Peer Reviewed Journal]COPYRIGHT 2015 Frontiers Research Foundation ;2015. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2015 Lee, Anand, Will, Adeyemi, Clasen, Blumenthal, Giedd, Daunhauer, Fidler and Edgin. 2015 Lee, Anand, Will, Adeyemi, Clasen, Blumenthal, Giedd, Daunhauer, Fidler and Edgin ;ISSN: 1662-5153 ;EISSN: 1662-5153 ;DOI: 10.3389/fnbeh.2015.00264 ;PMID: 26539087Full text available |
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Material Type: Article
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The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking studyJournal of neurodevelopmental disorders, 2022-08, Vol.14 (1), p.44-44, Article 44 [Peer Reviewed Journal]2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2022 ;ISSN: 1866-1947 ;EISSN: 1866-1955 ;DOI: 10.1186/s11689-022-09453-x ;PMID: 35918661Full text available |
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Material Type: Article
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Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of PregnancyMedicinski arhiv, 2017-04, Vol.71 (2), p.144-147 [Peer Reviewed Journal]Copyright Academy of Medical Sciences of Bosnia and Herzegovina 2017 ;Copyright: © 2017 Milenko Kolarski, Begzudin Ahmetovic, Maja Beres, Radomir Topic, Vedran Nikic, Ivana Kavecan, Semin Sabic 2017 ;ISSN: 0350-199X ;EISSN: 1986-5961 ;DOI: 10.5455/medarh.2017.71.144-147 ;PMID: 28790549Full text available |
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Material Type: Article
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Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18Case reports in pathology, 2018-01, Vol.2018, p.2839765-5 [Peer Reviewed Journal]Copyright © 2018 Sujal I. Shah et al. ;COPYRIGHT 2018 Hindawi Limited ;Copyright © 2018 Sujal I. Shah et al. 2018 ;ISSN: 2090-6781 ;EISSN: 2090-679X ;DOI: 10.1155/2018/2839765 ;PMID: 29707399Full text available |
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Material Type: Article
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45,X/47,XXX Mosaicism and Short StatureCase reports in pediatrics, 2015-01, Vol.2015, p.263253-3 [Peer Reviewed Journal]Copyright © 2015 Erica Everest et al. ;Copyright © 2015 Erica Everest et al. Erica Everest et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Copyright © 2015 Erica Everest et al. 2015 ;ISSN: 2090-6803 ;EISSN: 2090-6811 ;DOI: 10.1155/2015/263253 ;PMID: 26137340Full text available |
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Material Type: Article
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Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40‐year‐old woman with a mosaic Turner's karyotype (45,X/47,XXX)Acta obstetricia et gynecologica Scandinavica, 2003-08, Vol.82 (8), p.773-774 [Peer Reviewed Journal]ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1034/j.1600-0412.2003.00071.x ;PMID: 12848653Full text available |
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Material Type: Article
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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reportsReproductive medicine and biology, 2013-10, Vol.12 (4), p.193-195 [Peer Reviewed Journal]Japan Society for Reproductive Medicine 2013 ;The Japan Society for Reproductive Medicine ;Copyright John Wiley & Sons, Inc. Oct 2013 ;ISSN: 1445-5781 ;EISSN: 1447-0578 ;DOI: 10.1007/s12522-013-0158-9 ;PMID: 29699146Digital Resources/Online E-Resources |
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Material Type: Article
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21Journal of medical genetics, 1995-08, Vol.32 (8), p.650-653 [Peer Reviewed Journal]1995 INIST-CNRS ;Copyright BMJ Publishing Group LTD Aug 1995 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.32.8.650 ;PMID: 7473661 ;CODEN: JMDGAEFull text available |
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Material Type: Article
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Gilles de la Tourette's syndrome in a patient with 47(XXX) syndrome: a case reportJournal of medical case reports, 2011-11, Vol.5 (1), p.542-542, Article 542 [Peer Reviewed Journal]COPYRIGHT 2011 BioMed Central Ltd. ;COPYRIGHT 2011 BioMed Central Ltd. ;Copyright ©2011 Chiappedi et al; licensee BioMed Central Ltd. 2011 Chiappedi et al; licensee BioMed Central Ltd. ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/1752-1947-5-542 ;PMID: 22054059Full text available |
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Material Type: Article
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Counting‐based cell‐free DNA screening test fails to identify triploidy—A case reportClinical case reports, 2019-01, Vol.7 (1), p.90-93 [Peer Reviewed Journal]2018 The Authors. published by John Wiley & Sons Ltd. ;2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.1812 ;PMID: 30656016Full text available |
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Material Type: Article
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Fertility in 47,XXX and 45,X patientsJournal of medical genetics, 1978-04, Vol.15 (2), p.132-135 [Peer Reviewed Journal]Copyright BMJ Publishing Group LTD Apr 1978 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.15.2.132 ;PMID: 641947 ;CODEN: JMDGAEFull text available |