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1 |
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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2 |
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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3 |
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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4 |
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. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426Full text available |
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Material Type: Article
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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 |
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6 |
Material Type: Article
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21Journal of medical genetics, 1995-08, Vol.32 (8), p.650-653 [Peer Reviewed Journal]1995 INIST-CNRS ;Copyright BMJ Publishing Group LTD Aug 1995 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.32.8.650 ;PMID: 7473661 ;CODEN: JMDGAEFull text available |
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7 |
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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8 |
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. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000020984 ;PMID: 10720874Full text available |
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9 |
Material Type: Article
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Fertility in 47,XXX and 45,X patientsJournal of medical genetics, 1978-04, Vol.15 (2), p.132-135 [Peer Reviewed Journal]Copyright BMJ Publishing Group LTD Apr 1978 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.15.2.132 ;PMID: 641947 ;CODEN: JMDGAEFull text available |
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10 |
Material Type: Article
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A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXYHuman genetics, 1984-01, Vol.66 (4), p.367-369 [Peer Reviewed Journal]1985 INIST-CNRS ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00287644 ;PMID: 6586638 ;CODEN: HUGEDQFull text available |
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11 |
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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12 |
Material Type: Article
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Antenatal diagnosis of an XXX female. A dilemma for genetic counselingThe Western journal of medicine, 1975-07, Vol.123 (1), p.17-21 [Peer Reviewed Journal]ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778Full text available |
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13 |
Material Type: Article
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Pathomorphological changes in an early spontaneous abortus with triploidy (69, XXX)Human genetics, 1976-05, Vol.32 (2), p.211-215 [Peer Reviewed Journal]ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/BF00291507 ;PMID: 1270081Full 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 ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000074260 ;PMID: 14646418Full text available |
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15 |
Material Type: magazinearticle
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XXX-posed: how much sex and violence is too much?The Camping magazine, 2015-11, Vol.88 (6), p.34COPYRIGHT 2015 American Camping Association ;COPYRIGHT 2015 American Camping Association ;Copyright American Camping Association Nov/Dec 2015 ;ISSN: 0740-4131 ;CODEN: CMMGBHFull text available |
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16 |
Material Type: Article
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Clinical details, cytogenic studies,and cellular physiology of a 69, XXX fetus, with comments on the biological effect of triploidy in manJournal of medical genetics, 1976-10, Vol.13 (5), p.371-380 [Peer Reviewed Journal]Copyright BMJ Publishing Group LTD Oct 1976 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.13.5.371 ;PMID: 1034015 ;CODEN: JMDGAEFull text available |
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17 |
Material Type: Article
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Assessment of Fetal Sex Chromosome Aneuploidy Using Directed Cell-Free DNA AnalysisFetal diagnosis and therapy, 2014-02, Vol.35 (1), p.1-6 [Peer Reviewed Journal]2013 S. Karger AG, Basel ;2013 S. Karger AG, Basel. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000357198 ;PMID: 24335155Full text available |
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18 |
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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19 |
Material Type: Article
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Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testingClinical chemistry (Baltimore, Md.), 2014-01, Vol.60 (1), p.251-259 [Peer Reviewed Journal]COPYRIGHT 2014 American Association for Clinical Chemistry, Inc. ;Copyright American Association for Clinical Chemistry Jan 2014 ;ISSN: 0009-9147 ;EISSN: 1530-8561 ;DOI: 10.1373/clinchem.2013.215145 ;PMID: 24193117Full text available |
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20 |
Material Type: Article
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Prenatal Diagnosis of Sex Chromosome Abnormalities: The 8-Year Experience of a Single Medical CenterFetal diagnosis and therapy, 2008-01, Vol.23 (1), p.76-81 [Peer Reviewed Journal]2007 S. Karger AG, Basel ;2008 INIST-CNRS ;(c) 2007 S. Karger AG, Basel ;Copyright (c) 2007 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000109231 ;PMID: 17934303Full text available |