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1 |
Material Type: Article
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A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 yearsChild neuropsychology, 2022-02, Vol.28 (2), p.171-196 [Peer Reviewed Journal]2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021 ;ISSN: 0929-7049 ;EISSN: 1744-4136 ;DOI: 10.1080/09297049.2021.1960959Digital Resources/Online E-Resources |
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2 |
Material Type: Article
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Early symptoms of autism spectrum disorder (ASD) in 1–8 year old children with sex chromosome trisomies (XXX, XXY, XYY), and the predictive value of joint attentionEuropean child & adolescent psychiatry, 2023-11, Vol.32 (11), p.2323-2334 [Peer Reviewed Journal]The Author(s) 2022 ;ISSN: 1018-8827 ;EISSN: 1435-165X ;DOI: 10.1007/s00787-022-02070-yDigital Resources/Online E-Resources |
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3 |
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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4 |
Material Type: Article
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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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5 |
Material Type: Article
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Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic reviewDevelopmental medicine and child neurology, 2010-02, Vol.52 (2), p.119-129 [Peer Reviewed Journal]The Authors. Journal compilation © Mac Keith Press 2010 ;Copyright Mac Keith Press Feb 2010 ;Copyright © 2010 Mac Keith Press ;ISSN: 0012-1622 ;EISSN: 1469-8749 ;DOI: 10.1111/j.1469-8749.2009.03545.x ;PMID: 20059514 ;CODEN: DMCNAWFull text available |
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6 |
Material Type: Article
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Detection of VEGF-A(xxx)b isoforms in human tissuesPloS one, 2013, Vol.8 (7), p.e68399 [Peer Reviewed Journal]EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0068399 ;PMID: 23935865Full text available |
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7 |
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 |
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8 |
Material Type: Article
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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. ;ISSN: 1601-1848 ;EISSN: 1601-183X ;DOI: 10.1111/gbb.12180 ;PMID: 25287572 ;CODEN: GBBEAOFull text available |
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9 |
Material Type: Article
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre studyPrenatal 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: 27018091Full text available |
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10 |
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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11 |
Material Type: Article
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International Union of Pharmacology. XXX. Update on Chemokine Receptor NomenclaturePharmacological reviews, 2002-06, Vol.54 (2), p.227-229 [Peer Reviewed Journal]ISSN: 0031-6997 ;EISSN: 1521-0081 ;DOI: 10.1124/pr.54.2.227 ;PMID: 12037138Full text available |
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12 |
Material Type: Article
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Crown heights in the permanent teeth of 47,XXY males and 47,XXX femalesActa odontologica Scandinavica, 2022-04, Vol.80 (3), p.218-225 [Peer Reviewed Journal]2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Acta Odontologica Scandinavica Society. 2021 ;ISSN: 0001-6357 ;EISSN: 1502-3850 ;DOI: 10.1080/00016357.2021.1989031Digital Resources/Online E-Resources |
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13 |
Material Type: Article
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Structural and pragmatic language in young children with sex chromosome trisomy (XXX, XXY, XYY): Predictive value for neurobehavioral problems one year laterClinical neuropsychologist, 2023-04, Vol.37 (3), p.650-675 [Peer Reviewed Journal]2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2022 ;ISSN: 1385-4046 ;EISSN: 1744-4144 ;DOI: 10.1080/13854046.2022.2067078Digital Resources/Online E-Resources |
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14 |
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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15 |
Material Type: Article
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Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanomaBritish journal of cancer, 2007-07, Vol.97 (2), p.223-230 [Peer Reviewed Journal]ISSN: 0007-0920 ;EISSN: 1532-1827 ;DOI: 10.1038/sj.bjc.6603839 ;PMID: 17595666Full text available |
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16 |
Material Type: Article
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Arg-Phe-Phe d‑Amino Acid Stereochemistry Scan in the Macrocyclic Agouti-Related Protein Antagonist Scaffold c[Pro-Arg-Phe-Phe-Xxx-Ala-Phe-DPro] Results in Unanticipated Melanocortin‑1 Receptor Agonist ProfilesACS chemical neuroscience, 2018-12, Vol.9 (12), p.3015-3023 [Peer Reviewed Journal]ISSN: 1948-7193 ;EISSN: 1948-7193 ;DOI: 10.1021/acschemneuro.8b00218 ;PMID: 29924583Full text available |
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17 |
Material Type: Article
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The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking studyJournal 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: 35918661Full text available |
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18 |
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 |
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19 |
Material Type: Article
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Mortality and incidence in women with 47,XXX and variantsAmerican journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Peer Reviewed Journal]Copyright © 2010 Wiley‐Liss, Inc. ;Copyright 2010 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.33214 ;PMID: 20101696Full text available |
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20 |
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 |