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1	Material Type: Article	A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21 Molecular 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: 32463164 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	Material Type: Article	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 fetus Archives 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: 23625330 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
3	Material Type: Article	TRIPLOIDÍA 69,XXX EN RELACIÓN A LA EXPOSICIÓN PATERNA AL FINASTERIDE BAG. Journal of basic and applied genetics, 2017-01, Vol.28, p.119 [Peer Reviewed Journal] ISSN: 1666-0390 ;EISSN: 1852-6233 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study Orphanet 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: 30642344 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	Double trisomy 48,XXX,+18 with multiple dysmorphic features World journal of pediatrics : WJP, 2015-02, Vol.11 (1), p.83 [Peer Reviewed Journal] EISSN: 1867-0687 ;DOI: 10.1007/s12519-015-0005-7 ;PMID: 25822702 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
6	Material Type: Article	Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study Prenatal 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: 27018091 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
7	Material Type: Article	45,X/47,XXX Mosaicism and Short Stature Case 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: 26137340 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
8	Material Type: Article	Sonographic, Cytogenetic and DNA Analysis in Four 69,XXX Fetuses Diagnosed in the Second Trimester Fetal 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. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Morphological features and measurements in a human fetus with karyotype 69, XXX: comparison with fetuses of the same CRL, without chromosomal anomalies Italian journal of anatomy and embryology, 2001-07, Vol.106 (3), p.261-272 [Peer Reviewed Journal] ISSN: 1122-6714 ;PMID: 11767202 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
10	Material Type: Article	Management of Pregnancy Achieved by Oocyte Donation to a Woman with 47,XXX and POF Journal of mammalian ova research, 2011-10, Vol.28 (3), p.139-142 ISSN: 1341-7738 ;EISSN: 1347-5878 ;DOI: 10.1274/jmor.28.139 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
11	Material Type: Article	Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX The 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: 23937348 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review The 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: 20923275 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
13	Material Type: Article	Long-term survival in a 69,XXX triploid premature infant American journal of medical genetics. Part A, 2008-06, Vol.146A (12), p.1618-1621 [Peer Reviewed Journal] Copyright © 2008 Wiley‐Liss, Inc. ;2008 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.32352 ;PMID: 18478596 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
14	Material Type: Article	Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases Prenatal 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: 15614873 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
15	Material Type: Article	Noninvasive prenatal testing for assessing foetal sex chromosome aneuploidy: a retrospective study of 45,773 cases Molecular cytogenetics, 2021-01, Vol.14 (1), p.1-1, Article 1 [Peer Reviewed Journal] COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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) 2021 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-020-00521-2 ;PMID: 33407708 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	The epidemiology of sex chromosome abnormalities American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.202 2020 Wiley Periodicals LLC. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31805 ;PMID: 32506765 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by
17	Material Type: Article	Management of Pregnancy Achieved by Oocyte Donation to a Woman with 47,XXX and POF Journal of Mammalian Ova Research, 2011-10, Vol.28 (3), p.139-143 ISSN: 1341-7738 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
18	Material Type: Article	Diagnóstico prenatal de un feto con doble trisomía con cariotipo 48 XXX +18: reporte de un caso Ginecologia y obstetricia de Mexico, 2018-12, Vol.86 (12), p.810-814 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0300-9041 ;DOI: 10.24245/gom.v86i12.1814 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature Fetal 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: 20160426 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
20	Material Type: Article	A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy Prenatal diagnosis, 2023-02, Vol.43 (2), p.133 [Peer Reviewed Journal] 2023 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6298 ;PMID: 36588186 Digital Resources/Online E-Resources Services Details Recommendations Reviews Times Cited Citations Cited by

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Results 1 - 20 of 1,798 for All Library Resources

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: 23625330

ISSN: 1666-0390 ;EISSN: 1852-6233

EISSN: 1867-0687 ;DOI: 10.1007/s12519-015-0005-7 ;PMID: 25822702

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: 27018091

2000 S. Karger AG, Basel ;2000 INIST-CNRS ;Copyright 2000 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874

ISSN: 1122-6714 ;PMID: 11767202

ISSN: 1341-7738 ;EISSN: 1347-5878 ;DOI: 10.1274/jmor.28.139

2011 Informa UK, Ltd. 2011 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.3109/14767058.2010.520769 ;PMID: 20923275

Copyright © 2008 Wiley‐Liss, Inc. ;2008 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.32352 ;PMID: 18478596

Copyright © 2004 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1047 ;PMID: 15614873

2020 Wiley Periodicals LLC. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31805 ;PMID: 32506765

ISSN: 1341-7738

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0300-9041 ;DOI: 10.24245/gom.v86i12.1814

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: 20160426

2023 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6298 ;PMID: 36588186

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