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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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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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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 |
| 3 |
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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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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 |
| 5 |
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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 |
| 6 |
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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 |
| 7 |
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Sex chromosome trisomies in Europe: prevalence, prenatal detection and outcome of pregnancyEuropean journal of human genetics : EJHG, 2011-02, Vol.19 (2), p.231-234 [Peer Reviewed Journal]2015 INIST-CNRS ;Copyright Nature Publishing Group Feb 2011 ;Copyright © 2011 Macmillan Publishers Limited 2011 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2010.148 ;PMID: 20736977Full text available |
| 8 |
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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 |
| 9 |
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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 ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000074260 ;PMID: 14646418Full text available |
| 10 |
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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNAAmerican journal of obstetrics and gynecology, 2014-10, Vol.211 (4), p.365.e1 [Peer Reviewed Journal]Copyright © 2014 Elsevier Inc. All rights reserved. ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2014.03.042 ;PMID: 24657131Digital Resources/Online E-Resources |
| 11 |
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Prevalence of the triple X syndrome in phenotypically normal women with premature ovarian failure and its association with autoimmune thyroid disordersFertility and sterility, 2003-10, Vol.80 (4), p.1052-1054 [Peer Reviewed Journal]2003 American Society for Reproductive Medicine ;2004 INIST-CNRS ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/S0015-0282(03)01121-X ;PMID: 14556833 ;CODEN: FESTASFull text available |
| 12 |
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Replacing the Combined Test by Cell-Free DNA Testing in Screening for Trisomies 21, 18 and 13: Impact on the Diagnosis of Other Chromosomal AbnormalitiesFetal diagnosis and therapy, 2014-06, Vol.35 (3), p.174-184 [Peer Reviewed Journal]2014 S. Karger AG, Basel ;2014 S. Karger AG, Basel. ;ISSN: 1015-3837 ;ISBN: 9783318026924 ;ISBN: 3318026921 ;EISSN: 1421-9964 ;EISBN: 331802693X ;EISBN: 9783318026931 ;DOI: 10.1159/000358388 ;PMID: 24525399Full text available |
| 13 |
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Breastfeeding at 1, 3 and 6 Months after Birth According to the Mode of Birth: A Correlation StudyInternational journal of environmental research and public health, 2020-09, Vol.17 (18), p.6828 [Peer Reviewed Journal]2020 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 (http://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. ;2020 by the authors. 2020 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph17186828 ;PMID: 32962055Full text available |
| 14 |
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An assessment of the analytical performance of non‐invasive prenatal testing (NIPT) in detecting sex chromosome aneuploidies: 34,717‐patient sample in a single prenatal diagnosis Centre in ChinaThe journal of gene medicine, 2021-09, Vol.23 (9), p.e3362-n/a [Peer Reviewed Journal]2021 John Wiley & Sons, Ltd. ;ISSN: 1099-498X ;EISSN: 1521-2254 ;DOI: 10.1002/jgm.3362 ;PMID: 33973298Digital Resources/Online E-Resources |
| 15 |
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Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in IranFetal diagnosis and therapy, 2020-03, Vol.47 (3), p.220-227 [Peer Reviewed Journal]2019 S. Karger AG, Basel ;2019 S. Karger AG, Basel. ;COPYRIGHT 2020 S. Karger AG ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000501014 ;PMID: 31487708Digital Resources/Online E-Resources |
| 16 |
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Chromosomal abnormalities in couples with history of recurrent abortionRevista Brasileira de ginecologia e obstetrícia, 2009-02, Vol.31 (2), p.68-74 [Peer Reviewed Journal]EISSN: 1806-9339 ;DOI: 10.1590/S0100-72032009000200004 ;PMID: 19407911Full text available |
| 17 |
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Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologiesBirth defects research. A Clinical and molecular teratology, 2009-01, Vol.85 (1), p.58-62 [Peer Reviewed Journal]Copyright © 2008 Wiley‐Liss, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.20547 ;PMID: 19107956Full text available |
| 18 |
Material Type: Article
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Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experienceBMC research notes, 2020-03, Vol.13 (1), p.167-167, Article 167 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. 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) 2020 ;ISSN: 1756-0500 ;EISSN: 1756-0500 ;DOI: 10.1186/s13104-020-05009-1 ;PMID: 32188487Full text available |
| 19 |
Material Type: Article
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Normal nuchal thickness in the midtrimester indicates reduced risk of Down syndrome in pregnancies with abnormal triple-screen resultsAmerican journal of obstetrics and gynecology, 1995-10, Vol.173 (4), p.1106-1110 [Peer Reviewed Journal]1996 INIST-CNRS ;ISSN: 0002-9378 ;EISSN: 1097-6868 ;DOI: 10.1016/0002-9378(95)91334-3 ;PMID: 7485301 ;CODEN: AJOGAHFull text available |
| 20 |
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In vitro fertilization and pregnancy outcomes of women with X chromosome abnormality: A case seriesBirth defects research, 2024-05, Vol.116 (5), p.e23492024 Wiley Periodicals LLC. ;EISSN: 2472-1727 ;DOI: 10.1002/bdr2.2349 ;PMID: 38778782Digital Resources/Online E-Resources |
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