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1 |
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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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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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3 |
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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4 |
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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5 |
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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6 |
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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7 |
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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8 |
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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9 |
Material Type: Article
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Case report of a 22-week fetus with 47,XXX karyotype and multiple lower mesodermal defectsPediatric and developmental pathology, 1999-01, Vol.2 (1), p.58-61 [Peer Reviewed Journal]ISSN: 1093-5266 ;EISSN: 1615-5742 ;DOI: 10.1007/s100249900090 ;PMID: 9841707Digital Resources/Online E-Resources |
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10 |
Material Type: Article
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Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosisEuropean journal of pediatrics, 2010-10, Vol.169 (10), p.1255-1261 [Peer Reviewed Journal]Springer-Verlag 2010 ;2015 INIST-CNRS ;ISSN: 0340-6199 ;EISSN: 1432-1076 ;DOI: 10.1007/s00431-010-1221-8 ;PMID: 20473517 ;CODEN: EJPEDTFull text available |
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11 |
Material Type: Article
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Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second TrimesterFetal diagnosis and therapy, 2000-03, Vol.15 (2), p.97-101 [Peer Reviewed Journal]2000 S. Karger AG, Basel ;2000 INIST-CNRS ;Copyright 2000 S. Karger AG, Basel. ;Copyright (c) 2000 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874Full text available |
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12 |
Material Type: Article
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Evidence of a second gamete fusion after the first cleavage of the zygote in a 47,XX, + 18/70,XXX, + 18 mosaic. A remarkable diploid-triploid discrepancy after CVSPrenatal diagnosis, 1993-04, Vol.13 (4), p.301-306 [Peer Reviewed Journal]Copyright © 1993 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1970130409 ;PMID: 8506231Full text available |
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13 |
Material Type: Article
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Prenatal diagnosis and gonadal findings in X/XXX mosaicismJournal of medical genetics, 1977-04, Vol.14 (2), p.120-123 [Peer Reviewed Journal]Copyright BMJ Publishing Group LTD Apr 1977 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.14.2.120 ;PMID: 856232 ;CODEN: JMDGAEFull text available |
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14 |
Material Type: Article
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Prenatal Diagnosis of Congenital Diaphragmatic Hernia in a McFadden Kalousek Type 2 Triploid FetusFetal diagnosis and therapy, 2004-01, Vol.19 (1), p.49-51 [Peer Reviewed Journal]2004 S. Karger AG, Basel ;2004 INIST-CNRS ;Copyright 2004 S. Karger AG, Basel ;Copyright (c) 2004 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000074260 ;PMID: 14646418Full text available |
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15 |
Material Type: Article
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Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing PopulationPloS one, 2016-08, Vol.11 (8), p.e0161045-e0161045 [Peer Reviewed Journal]COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Samango-Sprouse et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Samango-Sprouse et al 2016 Samango-Sprouse et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0161045 ;PMID: 27512996Full text available |
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16 |
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Variation in the decision to terminate pregnancy in the setting of fetal aneuploidyPrenatal diagnosis, 2006-08, Vol.26 (8), p.667-671 [Peer Reviewed Journal]Copyright © 2006 John Wiley & Sons, Ltd. ;2006 INIST-CNRS ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1462 ;PMID: 16724363 ;CODEN: PRDIDMFull text available |
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17 |
Material Type: Article
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Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancyUltrasound in obstetrics & gynecology, 2015-01, Vol.45 (1), p.55 [Peer Reviewed Journal]Copyright © 2014 ISUOG. Published by John Wiley & Sons Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.13460 ;PMID: 25044397Digital Resources/Online E-Resources |
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18 |
Material Type: Article
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Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective studyPrenatal diagnosis, 2017-06, Vol.37 (6), p.583 [Peer Reviewed Journal]2017 John Wiley & Sons, Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.5051 ;PMID: 28406537Digital Resources/Online E-Resources |
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19 |
Material Type: Article
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Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implicationsMolecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1833-n/a [Peer Reviewed Journal]2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. 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/mgg3.1833 ;PMID: 34738344Full text available |
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20 |
Material Type: Article
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Assessing the role of placental trisomy in preeclampsia and intrauterine growth restrictionPrenatal diagnosis, 2010-01, Vol.30 (1), p.1-8 [Peer Reviewed Journal]Copyright © 2009 John Wiley & Sons, Ltd. ;2015 INIST-CNRS ;Copyright (c) 2009 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;ISSN: 1097-0223 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.2409 ;PMID: 19918961 ;CODEN: PRDIDMFull text available |