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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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xxx
xxx
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xxx

Ploughshares, 2013-12, Vol.39 (4), p.114-115

2013 Emerson College ;Copyright © Ploughshares at Emerson College ;COPYRIGHT 2013 Ploughshares, Inc. ;COPYRIGHT 2013 Ploughshares, Inc. ;Copyright Ploughshares Winter 2013/2014 ;ISSN: 0048-4474 ;ISSN: 2162-0903 ;EISSN: 2162-0903 ;DOI: 10.1353/plo.2013.0118

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3
Risk factors associated with intubation and readmissions in patients with angioedema: A single-center experience al. / Ann Allergy Asthma Immunol 127 (2021) xxx-xxx"?
Risk factors associated with intubation and readmissions in patients with angioedema: A single-center experience al. / Ann Allergy Asthma Immunol 127 (2021) xxx-xxx"?
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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: 34352359

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4
A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 years
A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 years
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A cross-sectional study of early language abilities in children with sex chromosome trisomy (XXY, XXX, XYY) aged 1-6 years

Child 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: 34346838

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5
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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6
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 attention
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 attention
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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 attention

European 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: 36107256

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7
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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8
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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9
A review of neurocognitive functioning and risk for psychopathology in sex chromosome trisomy (47,XXY, 47,XXX, 47, XYY)
A review of neurocognitive functioning and risk for psychopathology in sex chromosome trisomy (47,XXY, 47,XXX, 47, XYY)
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A review of neurocognitive functioning and risk for psychopathology in sex chromosome trisomy (47,XXY, 47,XXX, 47, XYY)

Current opinion in psychiatry, 2019-03, Vol.32 (2), p.79 [Peer Reviewed Journal]

EISSN: 1473-6578 ;DOI: 10.1097/yco.0000000000000471 ;PMID: 30689602

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10
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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11
Potent μ-Opioid Receptor Agonists from Cyclic Peptides Tyr-c[D-Lys-Xxx-Tyr-Gly]: Synthesis, Biological, and Structural Evaluation
Potent μ-Opioid Receptor Agonists from Cyclic Peptides Tyr-c[D-Lys-Xxx-Tyr-Gly]: Synthesis, Biological, and Structural Evaluation
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Potent μ-Opioid Receptor Agonists from Cyclic Peptides Tyr-c[D-Lys-Xxx-Tyr-Gly]: Synthesis, Biological, and Structural Evaluation

Journal of medicinal chemistry, 2016-02, Vol.59 (3), p.1239 [Peer Reviewed Journal]

EISSN: 1520-4804 ;DOI: 10.1021/acs.jmedchem.5b01899 ;PMID: 26789491

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12
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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13
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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14
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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15
Detection of VEGF-A(xxx)b isoforms in human tissues
Detection of VEGF-A(xxx)b isoforms in human tissues
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Detection of VEGF-A(xxx)b isoforms in human tissues

PloS one, 2013, Vol.8 (7), p.e68399 [Peer Reviewed Journal]

EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0068399 ;PMID: 23935865

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16
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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17
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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18
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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19
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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20
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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