Results 1 - 20 of 1,377 for All Library Resources
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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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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 |
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case reportMedicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Peer Reviewed Journal]Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 2022 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000031443 ;PMID: 36316845Full text available |
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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 |
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndromeGenes, brain and behavior, 2014-11, Vol.13 (8), p.841-849 [Peer Reviewed Journal]Published 2014. This article is a U.S. Government work and is in the public domain in the USA. ;2014 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12180 ;PMID: 25287572 ;CODEN: GBBEAOFull text available |
| 5 |
Material Type: Article
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Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXXGenes, brain and behavior, 2015-02, Vol.14 (2), p.200-208 [Peer Reviewed Journal]2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society ;2015 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society. ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12203 ;PMID: 25684214 ;CODEN: GBBEAOFull text available |
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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 |
| 7 |
Material Type: Article
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovariesClinical 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: 31183102Full text available |
| 8 |
Material Type: Article
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LP-105 Synergistic effect of extra X chromosome in the development of systemic lupus erythematosus in klinefelter syndrome karyotype 47, XXY and karyotype 47, XXX femalesLupus science & medicine, 2023-07, Vol.10 (Suppl 1), p.A127-A127 [Peer Reviewed Journal]2023 Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2053-8790 ;DOI: 10.1136/lupus-2023-KCR.207Full text available |
| 9 |
Material Type: Article
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic WomanInternal Medicine, 2014, Vol.53(7), pp.783-787 [Peer Reviewed Journal]2014 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.53.1325 ;PMID: 24694497Full text available |
| 10 |
Material Type: Article
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Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literatureMolecular 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: 31070017Full text available |
| 11 |
Material Type: Article
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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,XXXGenes, 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: 34073864Full text available |
| 12 |
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 |
| 13 |
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 |
| 14 |
Material Type: Article
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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reportsReproductive medicine and biology, 2013-10, Vol.12 (4), p.193-195 [Peer Reviewed Journal]Japan Society for Reproductive Medicine 2013 ;The Japan Society for Reproductive Medicine ;Copyright John Wiley & Sons, Inc. Oct 2013 ;ISSN: 1445-5781 ;EISSN: 1447-0578 ;DOI: 10.1007/s12522-013-0158-9 ;PMID: 29699146Digital Resources/Online E-Resources |
| 15 |
Material Type: Article
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Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX MosaicismInternal Medicine, 2009, Vol.48(6), pp.447-453 [Peer Reviewed Journal]2009 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.48.1157 ;PMID: 19293545Full text available |
| 16 |
Material Type: Article
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Pituitary tumor in a woman with a 47,XXX karyotype--case reportMedical science monitor, 2001-03, Vol.7 (2), p.304-307ISSN: 1234-1010 ;EISSN: 1643-3750 ;PMID: 11257740Full text available |
| 17 |
Material Type: Article
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Doctors’ experiences of adverse events in secondary care: the professional and personal impactClinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Peer Reviewed Journal]2014 © 2014 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;2015 INIST-CNRS ;2014 Royal College of Physicians 2014 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.14-6-585 ;PMID: 25468840Full text available |
| 18 |
Material Type: Article
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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: 12848653Full text available |
| 19 |
Material Type: Article
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The parental origin of the extra X chromosome in 47,XXX femalesAmerican journal of human genetics, 1990-04, Vol.46 (4), p.754-761 [Peer Reviewed Journal]1991 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 2316522 ;CODEN: AJHGAGFull text available |
| 20 |
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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