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1	Material Type: Article	Sex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXX Endocrine Connections, 2023-08, Vol.12 (9), p.1-10 [Peer Reviewed Journal] the author(s) ;the author(s) 2023 the author(s) ;ISSN: 2049-3614 ;EISSN: 2049-3614 ;DOI: 10.1530/EC-22-0440 ;PMID: 37399523 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
2	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
3	Material Type: Article	A review of trisomy X (47,XXX) Orphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Peer Reviewed Journal] COPYRIGHT 2010 BioMed Central Ltd. ;COPYRIGHT 2010 BioMed Central Ltd. ;Copyright ©2010 Tartaglia et al; licensee BioMed Central Ltd. 2010 Tartaglia et al; licensee BioMed Central Ltd. ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/1750-1172-5-8 ;PMID: 20459843 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
4	Material Type: Article	Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome Journal 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: JMDGAE Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
5	Material Type: Article	Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX Genes, 2021-06, Vol.12 (6), p.798 [Peer Reviewed Journal] 2021 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 (https://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. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12060798 ;PMID: 34073864 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
6	Material Type: Article	Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature Molecular 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: 31070017 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
7	Material Type: Article	47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries Clinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Peer Reviewed Journal] 2019 The Authors. published by John Wiley & Sons Ltd. ;2019. This work is published 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. ;ISSN: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.2207 ;PMID: 31183102 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
8	Material Type: Article	The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study Journal of neurodevelopmental disorders, 2022-08, Vol.14 (1), p.44-44, Article 44 [Peer Reviewed Journal] 2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;2022. 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) 2022 ;ISSN: 1866-1947 ;EISSN: 1866-1955 ;DOI: 10.1186/s11689-022-09453-x ;PMID: 35918661 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
9	Material Type: Article	Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18 Case reports in pathology, 2018-01, Vol.2018, p.2839765-5 [Peer Reviewed Journal] Copyright © 2018 Sujal I. Shah et al. ;COPYRIGHT 2018 Hindawi Limited ;Copyright © 2018 Sujal I. Shah et al. 2018 ;ISSN: 2090-6781 ;EISSN: 2090-679X ;DOI: 10.1155/2018/2839765 ;PMID: 29707399 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
10	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
11	Material Type: Article	Prenatal diagnosis of fetal hydrops associated with Down's syndrome in a 40‐year‐old woman with a mosaic Turner's karyotype (45,X/47,XXX) Acta obstetricia et gynecologica Scandinavica, 2003-08, Vol.82 (8), p.773-774 [Peer Reviewed Journal] ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1034/j.1600-0412.2003.00071.x ;PMID: 12848653 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
12	Material Type: Article	Fertility in 47,XXX and 45,X patients Journal 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: JMDGAE Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
13	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
14	Material Type: Article	Prenatal diagnosis and gonadal findings in X/XXX mosaicism Journal 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: JMDGAE Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
15	Material Type: Article	Antenatal diagnosis of an XXX female. A dilemma for genetic counseling The Western journal of medicine, 1975-07, Vol.123 (1), p.17-21 [Peer Reviewed Journal] ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
16	Material Type: Article	A viable fetus presenting 68,XX[73]/69,XXX[27] triploid mosaicism Genetics and molecular biology, 1998-09, Vol.21 (3), p.307-310 [Peer Reviewed Journal] This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 1415-4757 ;ISSN: 1678-4685 ;EISSN: 1678-4685 ;DOI: 10.1590/S1415-47571998000300002 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
17	Material Type: Article	Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1 American journal of human genetics, 1981-07, Vol.33 (4), p.649-650 [Peer Reviewed Journal] ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 7258190 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
18	Material Type: Article	Triple x syndrome with short stature: case report and literature review Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2012-06, Vol.22 (2), p.269-273 [Peer Reviewed Journal] Copyright Tehran University of Medical Sciences Publications Jun 2012 ;2012 Iranian Journal of Pediatrics & Tehran University of Medical Sciences 2012 ;ISSN: 2008-2142 ;EISSN: 2008-2150 ;PMID: 23056899 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
19	Material Type: Article	Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population PloS 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: 27512996 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by
20	Material Type: Article	Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report Medicine (Baltimore), 2020-07, Vol.99 (29), p.e20848-e20848 [Peer Reviewed Journal] Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020848 ;PMID: 32702826 Full text available View Online Details Recommendations Reviews Times Cited External Links Citations Cited by

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Results 1 - 20 of 913 for All Library Resources

the author(s) ;the author(s) 2023 the author(s) ;ISSN: 2049-3614 ;EISSN: 2049-3614 ;DOI: 10.1530/EC-22-0440 ;PMID: 37399523

COPYRIGHT 2010 BioMed Central Ltd. ;COPYRIGHT 2010 BioMed Central Ltd. ;Copyright ©2010 Tartaglia et al; licensee BioMed Central Ltd. 2010 Tartaglia et al; licensee BioMed Central Ltd. ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/1750-1172-5-8 ;PMID: 20459843

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: JMDGAE

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: 31070017

Copyright © 2018 Sujal I. Shah et al. ;COPYRIGHT 2018 Hindawi Limited ;Copyright © 2018 Sujal I. Shah et al. 2018 ;ISSN: 2090-6781 ;EISSN: 2090-679X ;DOI: 10.1155/2018/2839765 ;PMID: 29707399

ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1034/j.1600-0412.2003.00071.x ;PMID: 12848653

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: JMDGAE

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: JMDGAE

ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 1415-4757 ;ISSN: 1678-4685 ;EISSN: 1678-4685 ;DOI: 10.1590/S1415-47571998000300002

ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 7258190

Copyright Tehran University of Medical Sciences Publications Jun 2012 ;2012 Iranian Journal of Pediatrics & Tehran University of Medical Sciences 2012 ;ISSN: 2008-2142 ;EISSN: 2008-2150 ;PMID: 23056899

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020848 ;PMID: 32702826

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