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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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The behavioral profile of children aged 1-5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.4442020 The Authors. American Journal of Medical Genetics Part C: Seminars in Medical Genetics published by Wiley Periodicals, Inc. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31788 ;PMID: 32432413Digital Resources/Online E-Resources |
| 2 |
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Early impact of X- and Y-chromosome variations (XXX, XXY, XYY) on social communication and social emotional development in 1-2-year-old childrenAmerican journal of medical genetics. Part A, 2022-07, Vol.188 (7), p.1943 [Peer Reviewed Journal]2022 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC. ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.62720 ;PMID: 35285124Digital Resources/Online E-Resources |
| 3 |
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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 |
| 4 |
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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 |
| 5 |
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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 |
| 6 |
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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 |
| 7 |
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X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterizationPsychiatry and clinical neurosciences, 2022-12, Vol.76 (12), p.667-673 [Peer Reviewed Journal]2022 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Psychiatry and Neurology. ;2022 The Authors. Psychiatry and Clinical Neurosciences published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Psychiatry and Neurology. ;2022. This article 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: 1323-1316 ;EISSN: 1440-1819 ;DOI: 10.1111/pcn.13474 ;PMID: 36073611Full text available |
| 8 |
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Chromosomes and causation of human cancer and leukemia XXX. Banding studies of primary intestinal tumorsCancer, 1978-01, Vol.41 (1), p.164-173 [Peer Reviewed Journal]Copyright © 1978 American Cancer Society ;ISSN: 0008-543X ;EISSN: 1097-0142 ;DOI: 10.1002/1097-0142(197801)41:1<164::AID-CNCR2820410125>3.0.CO;2-6 ;PMID: 626926Digital Resources/Online E-Resources |
| 9 |
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Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesisActa Paediatrica, 2011-06, Vol.100 (6), p.903-907 [Peer Reviewed Journal]2011 The Author(s)/Acta Pædiatrica © 2011 Foundation Acta Pædiatrica ;2015 INIST-CNRS ;2011 The Author(s)/Acta Paediatrica © 2011 Foundation Acta Paediatrica. ;Acta Pædiatrica © 2011 Foundation Acta Pædiatrica 2011 ;ISSN: 0803-5253 ;EISSN: 1651-2227 ;DOI: 10.1111/j.1651-2227.2011.02150.x ;PMID: 21418292Full text available |
| 10 |
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Early developmental impact of sex chromosome trisomies on attention deficit-hyperactivity disorder symptomology in young childrenAmerican journal of medical genetics. Part A, 2021-12, Vol.185 (12), p.3664 [Peer Reviewed Journal]2021 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC. ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.62418 ;PMID: 34240550Digital Resources/Online E-Resources |
| 11 |
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Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriageUltrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.472 [Peer Reviewed Journal]Copyright © 2015 ISUOG. Published by John Wiley & Sons Ltd. ;EISSN: 1469-0705 ;DOI: 10.1002/uog.14849 ;PMID: 25767059Digital Resources/Online E-Resources |
| 12 |
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Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implicationsMolecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1833-n/a [Peer Reviewed Journal]2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. 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/mgg3.1833 ;PMID: 34738344Full text available |
| 13 |
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Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studiesMolecular genetics & genomic medicine, 2021-05, Vol.9 (5), p.e1654-n/a [Peer Reviewed Journal]2021 The Authors. published by Wiley Periodicals LLC. ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. 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/mgg3.1654 ;PMID: 33755350Full text available |
| 14 |
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Health care resource utilization before and after perampanel initiation among patients with epilepsy in the United StatesEpilepsia (Copenhagen), 2017-10, Vol.58 (10), p.1742-1748 [Peer Reviewed Journal]Wiley Periodicals, Inc. © 2017 International League Against Epilepsy ;Wiley Periodicals, Inc. © 2017 International League Against Epilepsy. ;Copyright © 2017 International League Against Epilepsy ;ISSN: 0013-9580 ;EISSN: 1528-1167 ;DOI: 10.1111/epi.13857 ;PMID: 28741690Digital Resources/Online E-Resources |
| 15 |
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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaDevelopmental medicine and child neurology, 2014-04, Vol.56 (4), p.346-353 [Peer Reviewed Journal]2013 The Authors. published by John Wiley & Sons Ltd on behalf of Mac Keith Press. ;2013 The Authors. Developmental Medicine & Child Neurology published by John Wiley & Sons Ltd on behalf of Mac Keith Press. ;2013 The Authors. published by John Wiley & Sons Ltd on behalf of Mac Keith Press. 2013 ;ISSN: 0012-1622 ;EISSN: 1469-8749 ;DOI: 10.1111/dmcn.12294 ;PMID: 24117048Digital Resources/Online E-Resources |
| 16 |
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Identification of endothelial cell‐specific molecule‐1 as a potential serum marker for colorectal cancerCancer science, 2010-10, Vol.101 (10), p.2248-2253 [Peer Reviewed Journal]2010 Japanese Cancer Association ;2015 INIST-CNRS ;2010 Japanese Cancer Association. ;ISSN: 1347-9032 ;EISSN: 1349-7006 ;DOI: 10.1111/j.1349-7006.2010.01665.x ;PMID: 20735430Digital Resources/Online E-Resources |
| 17 |
Material Type: Article
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Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomyAmerican journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.2562020 The Authors. American Journal of Medical Genetics Part C: Seminars in Medical Genetics published by Wiley Periodicals LLC. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31791 ;PMID: 32452638Digital Resources/Online E-Resources |
| 18 |
Material Type: Article
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The anti-angiogenic VEGF isoform VEGF165b transiently increases hydraulic conductivity, probably through VEGF receptor 1 in vivoThe Journal of physiology, 2006-04, Vol.572 (1), p.243-257 [Peer Reviewed Journal]2006 The Journal of Physiology © 2006 The Physiological Society ;2006 The Authors. Journal compilation © 2006 The Physiological Society 2006 ;ISSN: 0022-3751 ;EISSN: 1469-7793 ;DOI: 10.1113/jphysiol.2005.103127 ;PMID: 16423853Full text available |
| 19 |
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Patient selection, cancer control, and complications after salvage local therapy for postradiation prostate-specific antigen failure : A systematic review of the literatureCancer, 2007-10, Vol.110 (7), p.1417-1428 [Peer Reviewed Journal]2007 INIST-CNRS ;ISSN: 0008-543X ;EISSN: 1097-0142 ;DOI: 10.1002/cncr.22941 ;PMID: 17694553 ;CODEN: CANCARDigital Resources/Online E-Resources |
| 20 |
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Single determination of C-reactive protein at the time of diagnosis predicts long-term outcome of patients with hepatocellular carcinomaHepatology (Baltimore, Md.), 2013-06, Vol.57 (6), p.2224 [Peer Reviewed Journal]Copyright © 2012 American Association for the Study of Liver Diseases. ;EISSN: 1527-3350 ;DOI: 10.1002/hep.26057 ;PMID: 22961713Digital Resources/Online E-Resources |
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