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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Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic reviewDevelopmental medicine and child neurology, 2010-02, Vol.52 (2), p.119-129 [Peer Reviewed Journal]The Authors. Journal compilation © Mac Keith Press 2010 ;Copyright Mac Keith Press Feb 2010 ;Copyright © 2010 Mac Keith Press ;ISSN: 0012-1622 ;EISSN: 1469-8749 ;DOI: 10.1111/j.1469-8749.2009.03545.x ;PMID: 20059514 ;CODEN: DMCNAWFull text available |
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2 |
Material Type: Article
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The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic studyGenetics in medicine, 2022-02, Vol.24 (2), p.475-487 [Peer Reviewed Journal]2021 American College of Medical Genetics and Genomics ;Copyright © 2021 American College of Medical Genetics and Genomics. Published by Elsevier Inc. All rights reserved. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1016/j.gim.2021.10.012 ;PMID: 34906506Digital Resources/Online E-Resources |
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3 |
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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4 |
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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5 |
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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6 |
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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7 |
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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8 |
Material Type: Article
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Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XXThe journal of obstetrics and gynaecology research, 2014-01, Vol.40 (1), p.259-262 [Peer Reviewed Journal]2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology ;2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology. ;ISSN: 1341-8076 ;EISSN: 1447-0756 ;DOI: 10.1111/jog.12131 ;PMID: 23937348Full text available |
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9 |
Material Type: Article
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Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature reviewThe journal of maternal-fetal & neonatal medicine, 2011-05, Vol.24 (4), p.668-672 [Peer Reviewed Journal]2011 Informa UK, Ltd. 2011 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.3109/14767058.2010.520769 ;PMID: 20923275Digital Resources/Online E-Resources |
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10 |
Material Type: Article
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Prenatal diagnosis of 47,XXXAmerican journal of obstetrics and gynecology, 2005-05, Vol.192 (5), p.1469 [Peer Reviewed Journal]ISSN: 0002-9378 ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2004.12.037 ;PMID: 15902140Digital Resources/Online E-Resources |
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11 |
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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12 |
Material Type: Article
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Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetusArchives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Peer Reviewed Journal]Springer-Verlag Berlin Heidelberg 2013 ;Archives of Gynecology and Obstetrics is a copyright of Springer, (2013). All Rights Reserved. ;ISSN: 0932-0067 ;EISSN: 1432-0711 ;DOI: 10.1007/s00404-013-2847-3 ;PMID: 23625330Full text available |
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13 |
Material Type: Article
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Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXXBirth defects research. A Clinical and molecular teratology, 2007-08, Vol.79 (8), p.612-613 [Peer Reviewed Journal]Copyright © 2007 Wiley‐Liss, Inc. ;2007 Wiley-Liss, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.20371 ;PMID: 17469201Full text available |
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14 |
Material Type: Article
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratoryAmerican journal of obstetrics and gynecology, 2017-12, Vol.217 (6), p.691.e1 [Peer Reviewed Journal]Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved. ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2017.10.005 ;PMID: 29032050Digital Resources/Online E-Resources |
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15 |
Material Type: Article
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A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early interventionClinical genetics, 2020-01, Vol.97 (1), p.156 [Peer Reviewed Journal]2019 The Authors. Clinical Genetics published by John Wiley & Sons Ltd. ;EISSN: 1399-0004 ;DOI: 10.1111/cge.13586 ;PMID: 31267526Digital Resources/Online E-Resources |
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16 |
Material Type: Article
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Incidence of sex chromosome aneuploidy in a prenatal population: 27-year longitudinal study in Northern ItalyUltrasound in obstetrics & gynecology, 2023-08, Vol.62 (2), p.266 [Peer Reviewed Journal]2023 International Society of Ultrasound in Obstetrics and Gynecology. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.26201 ;PMID: 36929222Digital Resources/Online E-Resources |
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17 |
Material Type: Article
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two casesPrenatal diagnosis, 2004-12, Vol.24 (12), p.1020-1021 [Peer Reviewed Journal]Copyright © 2004 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1047 ;PMID: 15614873Full text available |
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18 |
Material Type: Article
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Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the LiteratureFetal diagnosis and therapy, 2010-03, Vol.27 (2), p.113-117 [Peer Reviewed Journal]2010 S. Karger AG, Basel ;2015 INIST-CNRS ;2010 S. Karger AG, Basel. ;Copyright (c) 2010 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426Full text available |
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19 |
Material Type: Article
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Spontaneous pregnancy in a woman with 45,X/47,XXX mosaicism in both serum and germ cell lines. A case reportJournal of reproductive medicine, 2003-02, Vol.48 (2), p.121 [Peer Reviewed Journal]ISSN: 0024-7758 ;EISSN: 1943-3565 ;PMID: 12621797Digital Resources/Online E-Resources |
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20 |
Material Type: Article
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Prenatal diagnosis of double trisomy 48,XXX,+18 in the first trimesterJournal of ultrasound in medicine, 2005-05, Vol.24 (5), p.717 [Peer Reviewed Journal]ISSN: 0278-4297 ;EISSN: 1550-9613 ;DOI: 10.7863/jum.2005.24.5.717 ;PMID: 15840805Digital Resources/Online E-Resources |