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1
Generation XXX: Pornography Acceptance and Use among Emerging Adults
Generation XXX: Pornography Acceptance and Use among Emerging Adults
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Generation XXX: Pornography Acceptance and Use among Emerging Adults

Journal of adolescent research, 2008, Vol.23 (1), p.6 [Peer Reviewed Journal]

ISSN: 0743-5584 ;EISSN: 1552-6895 ;DOI: 10.1177/0743558407306348

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2
The behavioral profile of children aged 1-5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)
The behavioral profile of children aged 1-5 years with sex chromosome trisomy (47,XXX, 47,XXY, 47,XYY)
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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.444

2020 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: 32432413

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3
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome
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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 Syndrome

Arthritis & 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: 26713507

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4
Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females
Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females
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Epigenetic and transcriptomic consequences of excess X-chromosome material in 47,XXX syndrome-A comparison with Turner syndrome and 46,XX females

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.279

2020 Wiley Periodicals LLC. ;EISSN: 1552-4876 ;DOI: 10.1002/ajmg.c.31799 ;PMID: 32489015

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5
A review of trisomy X (47,XXX)
A review of trisomy X (47,XXX)
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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: 20459843

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6
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report
Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case report

Medicine (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: 36316845

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7
How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973
How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973
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How Much More XXX is Generation X Consuming? Evidence of Changing Attitudes and Behaviors Related to Pornography Since 1973

The Journal of sex research, 2016-01, Vol.53 (1), p.12-20 [Peer Reviewed Journal]

Copyright © The Society for the Scientific Study of Sexuality 2016 ;Copyright Society for the Scientific Study of Sexuality 2016 ;ISSN: 0022-4499 ;EISSN: 1559-8519 ;DOI: 10.1080/00224499.2014.1003773 ;PMID: 26169262 ;CODEN: JSXRAJ

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8
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review
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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9
Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI study
Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI study
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Resting-state functional connectivity in adults with 47,XXX: a 7 Tesla MRI study

Cerebral 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. ;The Author(s) 2022. Published by Oxford University Press. 2022 ;ISSN: 1047-3211 ;EISSN: 1460-2199 ;DOI: 10.1093/cercor/bhac410 ;PMID: 36255323

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10
The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic study
The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic study
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The comorbidity landscape of 47,XXX syndrome: A nationwide epidemiologic study

Genetics in medicine, 2022-02, Vol.24 (2), p.475-487 [Peer Reviewed Journal]

2021 American College of Medical Genetics and Genomics ;Copyright © 2021 American College of Medical Genetics and Genomics. Published by Elsevier Inc. All rights reserved. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1016/j.gim.2021.10.012 ;PMID: 34906506

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11
Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study
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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12
False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism
False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism
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False-negative trisomy 18 non-invasive prenatal test result due to 48,XXX,+18 placental mosaicism

Ultrasound in obstetrics & gynecology, 2014-04, Vol.43 (4), p.477 [Peer Reviewed Journal]

EISSN: 1469-0705 ;DOI: 10.1002/uog.13240 ;PMID: 24186002

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13
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome
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A case‐control study of brain structure and behavioral characteristics in 47,XXX syndrome

Genes, 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: GBBEAO

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14
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study

Prenatal 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: 27018091

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15
Executive dysfunction and the relation with behavioral problems in children with 47,XXY and 47,XXX
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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16
Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY
Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY
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Attention-deficit hyperactivity disorder symptoms in children and adolescents with sex chromosome aneuploidy: XXY, XXX, XYY, and XXYY

Journal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309 [Peer Reviewed Journal]

EISSN: 1536-7312 ;DOI: 10.1097/DBP.0b013e31824501c8 ;PMID: 22333574

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17
A case of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysis
A case of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysis
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A case of non-mosaic X trisomy (65,XXX) in a Thoroughbred mare confirmed by cytogenetic and molecular analysis

Journal of applied genetics, 2024-05, Vol.65 (2), p.395 [Peer Reviewed Journal]

2024. The Author(s), under exclusive licence to Institute of Plant Genetics Polish Academy of Sciences. ;EISSN: 2190-3883 ;DOI: 10.1007/s13353-024-00844-5 ;PMID: 38368284

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18
Crown heights in the permanent teeth of 47,XXY males and 47,XXX females
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 ;PMID: 34666610

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19
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
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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,+21

Molecular 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: 32463164

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20
Poor socio-economic status in 47,XXX --an unexpected effect of an extra X chromosome
Poor socio-economic status in 47,XXX --an unexpected effect of an extra X chromosome
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Poor socio-economic status in 47,XXX --an unexpected effect of an extra X chromosome

European 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: 23542668

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