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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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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: 20459843Full text available |
| 2 |
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 |
| 3 |
Material Type: Article
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Sex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXXEndocrine 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: 37399523Full text available |
| 4 |
Material Type: Article
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VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivoBritish journal of cancer, 2009-10, Vol.101 (7), p.1183 [Peer Reviewed Journal]EISSN: 1532-1827 ;DOI: 10.1038/sj.bjc.6605249 ;PMID: 19707198Full text available |
| 5 |
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 |
| 6 |
Material Type: Article
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombinationHuman molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Peer Reviewed Journal]1994 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/3.8.1365 ;PMID: 7987316Full text available |
| 7 |
Material Type: Conference Proceeding
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X chromosome dose and sex bias in autoimmune diseases: increased 47,XXX in systemic lupus erythematosus and Sjögren’s syndrome (BA4P.211)JOURNAL OF IMMUNOLOGY, 2014, Vol.192 (1_Supplement), p.46-46.2 [Peer Reviewed Journal]ISSN: 0022-1767 ;EISSN: 1550-6606 ;DOI: 10.4049/jimmunol.192.Supp.46.2Full text available |
| 8 |
Material Type: Article
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Limits to sustained energy intake. XXX. Constraint or restraint? Manipulations of food supply show peak food intake in lactation is constrainedJournal of experimental biology, 2020-04, Vol.223 (Pt 8) [Peer Reviewed Journal]2020. Published by The Company of Biologists Ltd. ;ISSN: 0022-0949 ;EISSN: 1477-9145 ;DOI: 10.1242/jeb.208314 ;PMID: 32139473Full text available |
| 9 |
Material Type: Article
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Pharmacological Properties of Traditional Medicine (XXX): Effects of Gyokuheifusan (玉屏風散) on Murine Antigen-Specific Antibody ProductionBiological and Pharmaceutical Bulletin, 2005, Vol.28(1), pp.110-113 [Peer Reviewed Journal]2005 The Pharmaceutical Society of Japan ;ISSN: 0918-6158 ;EISSN: 1347-5215 ;DOI: 10.1248/bpb.28.110 ;PMID: 15635173Full text available |
| 10 |
Material Type: Article
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular eventsRheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Peer Reviewed Journal]2005 INIST-CNRS ;Copyright Oxford University Press(England) Jul 2005 ;ISSN: 1462-0324 ;EISSN: 1462-0332 ;DOI: 10.1093/rheumatology/keh613 ;PMID: 15797975 ;CODEN: BJRHDFFull text available |
| 11 |
Material Type: Article
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Premature ovarian failure related to trisomy X: Two case reports with an aberrant 47, XXX karyotypeJournal of human reproductive sciences, 2021-01, Vol.14 (1), p.87-90 [Peer Reviewed Journal]COPYRIGHT 2021 Indian Society of Assisted Reproduction ;COPYRIGHT 2021 Medknow Publications and Media Pvt. Ltd. ;2021. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright: © 2021 Journal of Human Reproductive Sciences 2021 ;ISSN: 0974-1208 ;EISSN: 1998-4766 ;DOI: 10.4103/jhrs.JHRS_59_20 ;PMID: 34083998Full text available |
| 12 |
Material Type: Article
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69, XXX Karyotype Triploidy SyndromeJournal of the Turkish German Gynecological Association, 2016-05, Vol.17, p.S329 [Peer Reviewed Journal]Copyright Aves Yayincilik Ltd. STI. May 2016 ;ISSN: 1309-0399 ;EISSN: 1309-0380Full text available |
| 13 |
Material Type: Article
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Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney TransplantationAmerican journal of transplantation, 2016-01, Vol.16 (1), p.213-220 [Peer Reviewed Journal]Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons ;Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons. ;ISSN: 1600-6135 ;EISSN: 1600-6143 ;DOI: 10.1111/ajt.13434 ;PMID: 26317487Full text available |
| 14 |
Material Type: Article
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The craniofacial complex in 47, XXX femalesEuropean journal of orthodontics, 2005-08, Vol.27 (4), p.396-401 [Peer Reviewed Journal]ISSN: 0141-5387 ;EISSN: 1460-2210 ;DOI: 10.1093/ejo/cji016 ;PMID: 16043476 ;CODEN: EJOODKFull text available |
| 15 |
Material Type: Article
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Everyday executive functions in Down syndrome from early childhood to young adulthood: evidence for both unique and shared characteristics compared to youth with sex chromosome trisomy (XXX and XXY)Frontiers in behavioral neuroscience, 2015-10, Vol.9, p.264-264 [Peer Reviewed Journal]COPYRIGHT 2015 Frontiers Research Foundation ;2015. 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. ;Copyright © 2015 Lee, Anand, Will, Adeyemi, Clasen, Blumenthal, Giedd, Daunhauer, Fidler and Edgin. 2015 Lee, Anand, Will, Adeyemi, Clasen, Blumenthal, Giedd, Daunhauer, Fidler and Edgin ;ISSN: 1662-5153 ;EISSN: 1662-5153 ;DOI: 10.3389/fnbeh.2015.00264 ;PMID: 26539087Full text available |
| 16 |
Material Type: Article
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Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18Case 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: 29707399Full text available |
| 17 |
Material Type: Article
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Long survival in a 69,XXX triploid infant in GreeceGenetics and molecular research, 2005-12, Vol.4 (4), p.755-759 [Peer Reviewed Journal]ISSN: 1676-5680 ;EISSN: 1676-5680 ;PMID: 16475122Full text available |
| 18 |
Material Type: Article
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Phenotypic variability in 47, XXX patients: Clinical report of four new casesArchivos argentinos de pediatría, 2010-08, Vol.108 (4), p.e88-e91 [Peer Reviewed Journal]EISSN: 1668-3501 ;DOI: 10.1590/S0325-00752010000400012 ;PMID: 20672182Digital Resources/Online E-Resources |
| 19 |
Material Type: Article
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, IndiaJournal of genetics, 2008-12, Vol.87 (3), p.257-259 [Peer Reviewed Journal]Indian Academy of Sciences 2008 ;ISSN: 0022-1333 ;EISSN: 0973-7731 ;DOI: 10.1007/s12041-008-0039-x ;PMID: 19147910Full text available |
| 20 |
Material Type: Article
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Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotypeJournal of genetics, 2018-03, Vol.97 (1), p.337-340 [Peer Reviewed Journal]Indian Academy of Sciences 2018 ;COPYRIGHT 2018 Springer ;Journal of Genetics is a copyright of Springer, (2018). All Rights Reserved. ;ISSN: 0022-1333 ;EISSN: 0973-7731 ;DOI: 10.1007/s12041-018-0916-x ;PMID: 29666354Full text available |
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