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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
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Risk factors associated with intubation and readmissions in patients with angioedema: A single-center experience al. / Ann Allergy Asthma Immunol 127 (2021) xxx-xxx"?Annals of allergy, asthma, & immunology, 2021-12, Vol.127 (6), p.682 [Peer Reviewed Journal]Copyright © 2021 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved. ;EISSN: 1534-4436 ;DOI: 10.1016/j.anai.2021.07.023 ;PMID: 34352359Digital Resources/Online E-Resources |
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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: 10.1080/09297049.2021.1960959 ;PMID: 34346838Digital Resources/Online E-Resources |
| 3 |
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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's SyndromeArthritis & rheumatology (Hoboken, N.J.), 2016-05, Vol.68 (5), p.1290-1300 [Peer Reviewed Journal]2016, American College of Rheumatology ;2016, American College of Rheumatology. ;ISSN: 2326-5191 ;ISSN: 2326-5205 ;EISSN: 2326-5205 ;DOI: 10.1002/art.39560 ;PMID: 26713507Full text available |
| 4 |
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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 ;2022. The Author(s). ;The Author(s) 2022. 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: 1018-8827 ;EISSN: 1435-165X ;DOI: 10.1007/s00787-022-02070-y ;PMID: 36107256Digital Resources/Online E-Resources |
| 5 |
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The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic studyGenetics in medicine, 2022-02, Vol.24 (2), p.475 [Peer Reviewed Journal]Copyright © 2021 American College of Medical Genetics and Genomics. Published by Elsevier Inc. All rights reserved. ;EISSN: 1530-0366 ;DOI: 10.1016/j.gim.2021.10.012 ;PMID: 34906506Digital Resources/Online E-Resources |
| 6 |
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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 |
| 7 |
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 |
| 8 |
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 |
| 9 |
Material Type: Article
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Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYYJournal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309 [Peer Reviewed Journal]EISSN: 1536-7312 ;DOI: 10.1097/DBP.0b013e31824501c8 ;PMID: 22333574Digital Resources/Online E-Resources |
| 10 |
Material Type: Article
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Poor socio-economic status in 47,XXX --an unexpected effect of an extra X chromosomeEuropean journal of medical genetics, 2013-06, Vol.56 (6), p.286 [Peer Reviewed Journal]Copyright © 2013 Elsevier Masson SAS. All rights reserved. ;EISSN: 1878-0849 ;DOI: 10.1016/j.ejmg.2013.03.008 ;PMID: 23542668Digital Resources/Online E-Resources |
| 11 |
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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 |
| 12 |
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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 |
| 13 |
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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 |
| 14 |
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 |
| 15 |
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Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosisAmerican journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2870-2881 [Peer Reviewed Journal]2016 Wiley Periodicals, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.37688 ;PMID: 27644018Full text available |
| 16 |
Material Type: Article
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypesAmerican journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Peer Reviewed Journal]Copyright © 2001 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.10154 ;PMID: 11840512 ;CODEN: AJMGDAFull text available |
| 17 |
Material Type: Article
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Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)Acta odontologica Scandinavica, 2010-07, Vol.68 (4), p.223 [Peer Reviewed Journal]EISSN: 1502-3850 ;DOI: 10.3109/00016357.2010.490954 ;PMID: 20568965Digital Resources/Online E-Resources |
| 18 |
Material Type: Article
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The epidemiology of sex chromosome abnormalitiesAmerican journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.2022020 Wiley Periodicals LLC. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31805 ;PMID: 32506765Digital 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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A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early interventionClinical genetics, 2020-01, Vol.97 (1), p.156 [Peer Reviewed Journal]2019 The Authors. Clinical Genetics published by John Wiley & Sons Ltd. ;EISSN: 1399-0004 ;DOI: 10.1111/cge.13586 ;PMID: 31267526Digital Resources/Online E-Resources |
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