Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Generation XXX: Pornography Acceptance and Use among Emerging AdultsJournal of adolescent research, 2008, Vol.23 (1), p.6 [Peer Reviewed Journal]ISSN: 0743-5584 ;EISSN: 1552-6895 ;DOI: 10.1177/0743558407306348Digital Resources/Online E-Resources |
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Material Type: Article
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case reportMedicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Peer Reviewed Journal]Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000031443 ;PMID: 36316845Full text available |
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3 |
Material Type: Article
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How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973The Journal of sex research, 2016-01, Vol.53 (1), p.12-20 [Peer Reviewed Journal]Copyright © The Society for the Scientific Study of Sexuality 2016 ;Copyright Society for the Scientific Study of Sexuality 2016 ;ISSN: 0022-4499 ;EISSN: 1559-8519 ;DOI: 10.1080/00224499.2014.1003773 ;PMID: 26169262 ;CODEN: JSXRAJDigital Resources/Online E-Resources |
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4 |
Material Type: Article
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Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI studyCerebral cortex (New York, N.Y. 1991), 2023-04, Vol.33 (9), p.5210-5217 [Peer Reviewed Journal]The Author(s) 2022. Published by Oxford University Press. 2022 ;The Author(s) 2022. Published by Oxford University Press. ;ISSN: 1047-3211 ;EISSN: 1460-2199 ;DOI: 10.1093/cercor/bhac410 ;PMID: 36255323Full text available |
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5 |
Material Type: Article
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Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort studyOrphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Peer Reviewed Journal]COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;Copyright © 2019. 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). 2019 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-018-0976-2 ;PMID: 30642344Full text available |
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6 |
Material Type: Article
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndromeGenes, brain and behavior, 2014-11, Vol.13 (8), p.841-849 [Peer Reviewed Journal]Published 2014. This article is a U.S. Government work and is in the public domain in the USA. ;2014 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12180 ;PMID: 25287572 ;CODEN: GBBEAOFull text available |
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7 |
Material Type: Article
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre studyPrenatal diagnosis, 2016-06, Vol.36 (6), p.523-529 [Peer Reviewed Journal]2016 John Wiley & Sons, Ltd. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.4817 ;PMID: 27018091Full text available |
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8 |
Material Type: Article
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Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYYJournal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309 [Peer Reviewed Journal]EISSN: 1536-7312 ;DOI: 10.1097/DBP.0b013e31824501c8 ;PMID: 22333574Digital Resources/Online E-Resources |
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9 |
Material Type: Article
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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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10 |
Material Type: Article
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Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging studyJournal of neurodevelopmental disorders, 2022-02, Vol.14 (1), p.14-14, Article 14 [Peer Reviewed Journal]2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1866-1947 ;EISSN: 1866-1955 ;DOI: 10.1186/s11689-022-09425-1 ;PMID: 35196987Full text available |
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11 |
Material Type: Article
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Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYYJournal of community genetics, 2024-02, Vol.15 (1), p.75-83 [Peer Reviewed Journal]The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;ISSN: 1868-310X ;ISSN: 1868-6001 ;EISSN: 1868-6001 ;DOI: 10.1007/s12687-023-00682-8 ;PMID: 37864743Full text available |
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12 |
Material Type: Article
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Poor socio-economic status in 47,XXX --an unexpected effect of an extra X chromosomeEuropean journal of medical genetics, 2013-06, Vol.56 (6), p.286 [Peer Reviewed Journal]Copyright © 2013 Elsevier Masson SAS. All rights reserved. ;EISSN: 1878-0849 ;DOI: 10.1016/j.ejmg.2013.03.008 ;PMID: 23542668Digital Resources/Online E-Resources |
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13 |
Material Type: Article
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A Spontaneous Pregnancy in a Patient with Turner Syndrome with 45,X/47,XXX Mosaicism: A Case Report and Review of the LiteratureJournal of pediatric & adolescent gynecology, 2018-12, Vol.31 (6), p.651 [Peer Reviewed Journal]Copyright © 2018 North American Society for Pediatric and Adolescent Gynecology. Published by Elsevier Inc. All rights reserved. ;EISSN: 1873-4332 ;DOI: 10.1016/j.jpag.2018.07.005 ;PMID: 30012427Digital Resources/Online E-Resources |
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14 |
Material Type: Article
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False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicismUltrasound in obstetrics & gynecology, 2014-04, Vol.43 (4), p.477 [Peer Reviewed Journal]EISSN: 1469-0705 ;DOI: 10.1002/uog.13240 ;PMID: 24186002Digital Resources/Online E-Resources |
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15 |
Material Type: Article
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Spontaneous Sexual Development and Heavy Menstrual Bleeding in 45,X Monosomy and 45,X/47,XXX Mosaic Turner Syndrome and a Review of the LiteratureJournal of pediatric & adolescent gynecology, 2020-10, Vol.33 (5), p.602 [Peer Reviewed Journal]Copyright © 2020 North American Society for Pediatric and Adolescent Gynecology. Published by Elsevier Inc. All rights reserved. ;EISSN: 1873-4332 ;DOI: 10.1016/j.jpag.2020.04.002 ;PMID: 32315714Digital Resources/Online E-Resources |
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16 |
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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17 |
Material Type: Article
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic WomanInternal Medicine, 2014, Vol.53(7), pp.783-787 [Peer Reviewed Journal]2014 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.53.1325 ;PMID: 24694497Full text available |
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18 |
Material Type: Article
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Mortality and incidence in women with 47,XXX and variantsAmerican journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Peer Reviewed Journal]Copyright © 2010 Wiley‐Liss, Inc. ;Copyright 2010 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.33214 ;PMID: 20101696Full text available |
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19 |
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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20 |
Material Type: Article
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Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)Fish physiology and biochemistry, 2016-02, Vol.42 (1), p.193-202 [Peer Reviewed Journal]Springer Science+Business Media Dordrecht 2015 ;Springer Science+Business Media Dordrecht 2016 ;ISSN: 0920-1742 ;EISSN: 1573-5168 ;DOI: 10.1007/s10695-015-0129-7 ;PMID: 26373423Full text available |