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1
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
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Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review

Developmental 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: DMCNAW

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2
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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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 study

Orphanet 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: 30642344

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3
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX

Genes, 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: GBBEAO

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4
Crown heights in the permanent teeth of 47,XXY males and 47,XXX females
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Crown heights in the permanent teeth of 47,XXY males and 47,XXX females

Acta 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: 10.1080/00016357.2021.1989031

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5
Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
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Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)

Fish physiology and biochemistry, 2016-02, Vol.42 (1), p.193-202 [Peer Reviewed Journal]

Springer Science+Business Media Dordrecht 2015 ;Springer Science+Business Media Dordrecht 2016 ;ISSN: 0920-1742 ;EISSN: 1573-5168 ;DOI: 10.1007/s10695-015-0129-7 ;PMID: 26373423

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6
VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo
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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 vivo

British journal of cancer, 2009-10, Vol.101 (7), p.1183 [Peer Reviewed Journal]

EISSN: 1532-1827 ;DOI: 10.1038/sj.bjc.6605249 ;PMID: 19707198

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7
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

Human molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Peer Reviewed Journal]

1994 INIST-CNRS ;ISSN: 0964-6906 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/3.8.1365 ;PMID: 7987316

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8
Impact of tumor location on medulloblastoma subtyping and treatment (Commentary on teo et al., page xxx)
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Impact of tumor location on medulloblastoma subtyping and treatment (Commentary on teo et al., page xxx)

Pediatric blood & cancer, 2013-09, Vol.60 (9), p.1393-1394 [Peer Reviewed Journal]

Copyright © 2013 Wiley Periodicals, Inc. ;ISSN: 1545-5009 ;EISSN: 1545-5017 ;DOI: 10.1002/pbc.24549 ;PMID: 23606316

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9
Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee
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Article
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Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee

Clinical and experimental rheumatology, 2010-11, Vol.28 (6), p.803-805 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0392-856X ;EISSN: 1593-098X ;PMID: 21205458

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10
Long-term survival in a 69,XXX triploid premature infant
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Long-term survival in a 69,XXX triploid premature infant

American journal of medical genetics. Part A, 2008-06, Vol.146A (12), p.1618-1621 [Peer Reviewed Journal]

Copyright © 2008 Wiley‐Liss, Inc. ;2008 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.32352 ;PMID: 18478596

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11
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events

Rheumatology (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: BJRHDF

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12
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

American 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: AJMGDA

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13
Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells
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Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells

Cytogenetic and genome research, 2004, Vol.104 (1-4), p.277-282 [Peer Reviewed Journal]

Copyright 2003 S. Karger AG, Basel ;ISSN: 1424-8581 ;EISSN: 1424-859X ;DOI: 10.1159/000077502 ;PMID: 15162051

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14
Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation
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Article
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Presentation and Outcomes of C4d‐Negative Antibody‐Mediated Rejection After Kidney Transplantation

American 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: 26317487

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15
Sex chromosome aneuploidies
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Article
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Sex chromosome aneuploidies

Handbook of Clinical Neurology, 2018, Vol.147, p.355-376 [Peer Reviewed Journal]

2018 Elsevier B.V. ;ISSN: 0072-9752 ;ISBN: 0444632336 ;ISBN: 9780444632333 ;DOI: 10.1016/B978-0-444-63233-3.00024-5

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16
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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Article
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Doctors’ experiences of adverse events in secondary care: the professional and personal impact

Clinical 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: 25468840

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17
45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism
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45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditism

American journal of medical genetics. Part A, 2004-10, Vol.130A (3), p.311-314 [Peer Reviewed Journal]

Copyright © 2004 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.30258 ;PMID: 15378545

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18
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
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Article
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Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX

Chromosome research, 2004-01, Vol.12 (2), p.125-132 [Peer Reviewed Journal]

Kluwer Academic Publishers 2004. ;ISSN: 0967-3849 ;EISSN: 1573-6849 ;DOI: 10.1023/B:CHRO.0000013164.56757.bd ;PMID: 15053482

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19
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
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Article
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Prenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Peer Reviewed Journal]

Copyright © 2000 John Wiley & Sons, Ltd. ;Copyright 2000 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/1097-0223(200009)20:9<750::AID-PD900>3.0.CO;2-E ;PMID: 11015706

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20
The parental origin of the extra X chromosome in 47,XXX females
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The parental origin of the extra X chromosome in 47,XXX females

American 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: AJHGAG

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