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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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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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Material Type: Article
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Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI studyCerebral cortex (New York, N.Y. 1991), 2023-04, Vol.33 (9), p.5210-5217 [Peer Reviewed Journal]The Author(s) 2022. Published by Oxford University Press. 2022 ;The Author(s) 2022. Published by Oxford University Press. ;ISSN: 1047-3211 ;EISSN: 1460-2199 ;DOI: 10.1093/cercor/bhac410 ;PMID: 36255323Full text available |
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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. ;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 |
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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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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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Material Type: Article
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Altered subcortical and cortical brain morphology in adult women with 47,XXX: a 7-Tesla magnetic resonance imaging studyJournal of neurodevelopmental disorders, 2022-02, Vol.14 (1), p.14-14, Article 14 [Peer Reviewed Journal]2022. The Author(s). ;COPYRIGHT 2022 BioMed Central Ltd. ;The Author(s) 2022 ;ISSN: 1866-1947 ;EISSN: 1866-1955 ;DOI: 10.1186/s11689-022-09425-1 ;PMID: 35196987Full text available |
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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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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 |
10 |
Material Type: Book Chapter
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XXX SyndromeAtlas of Genetic Diagnosis and Counseling, 2017, p.3045-3050Springer Science+Business Media LLC 2017 ;ISBN: 1493924001 ;ISBN: 9781493924004 ;EISBN: 9781493924011 ;EISBN: 149392401X ;DOI: 10.1007/978-1-4939-2401-1_251 ;OCLC: 992941389 ;LCCallNum: RB1-214Full text available |
11 |
Material Type: Article
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Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the LiteratureFetal diagnosis and therapy, 2010-03, Vol.27 (2), p.113-117 [Peer Reviewed Journal]2010 S. Karger AG, Basel ;2015 INIST-CNRS ;2010 S. Karger AG, Basel. ;Copyright (c) 2010 S. Karger AG, Basel ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426Full text available |
12 |
Material Type: Article
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Female-to-male transsexual with 47,XXX karyotypeBiological psychiatry (1969), 2000-12, Vol.48 (11), p.1116-1117 [Peer Reviewed Journal]2000 Society of Biological Psychiatry ;2001 INIST-CNRS ;ISSN: 0006-3223 ;EISSN: 1873-2402 ;DOI: 10.1016/S0006-3223(00)00954-9 ;PMID: 11094147 ;CODEN: BIPCBFFull text available |
13 |
Material Type: Article
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Rett syndrome in a 47,XXX patient with a de novo MECP2 mutationAmerican journal of medical genetics. Part A, 2003-10, Vol.122A (3), p.223-226 [Peer Reviewed Journal]Copyright © 2003 Wiley‐Liss, Inc. ;Copyright 2003 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20320 ;PMID: 12966522Full text available |
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Material Type: Article
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Genetics of Childhood Disorders: XXX. Autoimmune Disorders, Part 3: Myasthenia Gravis and Rasmussen's EncephalitisJournal of the American Academy of Child and Adolescent Psychiatry, 2001-09, Vol.40 (9), p.1115-1117 [Peer Reviewed Journal]2001 The American Academy of Child and Adolescent Psychiatry ;2001 INIST-CNRS ;Copyright Lippincott Williams & Wilkins Sep 2001 ;ISSN: 0890-8567 ;EISSN: 1527-5418 ;DOI: 10.1097/00004583-200109000-00022 ;PMID: 11556637 ;CODEN: JAAPEEFull text available |
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Material Type: Article
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Neurofibromatosis complicated with XXX syndrome and renovascular hypertensionJournal of internal medicine, 1996-06, Vol.239 (6), p.531-535 [Peer Reviewed Journal]Blackwell Science Ltd ;1996 INIST-CNRS ;ISSN: 0954-6820 ;EISSN: 1365-2796 ;DOI: 10.1046/j.1365-2796.1996.422778000.x ;PMID: 8656147Full text available |
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Material Type: Article
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Deep-brain stimulation for dystonia: current indications and future orientationsFuture Neurology, 2014-01, Vol.9 (1), p.77-87 [Peer Reviewed Journal]COPYRIGHT 2014 Future Medicine Ltd. ;2014 Future Medicine Ltd ;ISSN: 1479-6708 ;EISSN: 1748-6971 ;DOI: 10.2217/fnl.13.69Full text available |
17 |
Material Type: Article
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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 |
18 |
Material Type: Article
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Duchenne muscular dystrophy in a girl with a 45, X/46, XX/47, XXX chromosome constitutionAmerican journal of medical genetics, 1986-10, Vol.25 (2), p.239-243 [Peer Reviewed Journal]Copyright © 1986 Wiley‐Liss, Inc., A Wiley Company ;1987 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320250207 ;PMID: 3777022 ;CODEN: AJMGDAFull text available |
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Material Type: Article
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XXX National Congress of the Italian Neurological Society. Palermo, October 28-November 1, 1997. AbstractsItalian journal of neurological sciences, 1997, Vol.18 (4 Suppl), p.1-149ISSN: 0392-0461 ;EISSN: 1126-5442 ;PMID: 9429588Full text available |
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Material Type: Article
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Mosaic XXX-XXXX sex chromosome complement. Case report and review of literatureJournal of mental deficiency research, 1970-06, Vol.14 (2), p.141-148ISSN: 0022-264X ;PMID: 5512214Full text available |