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Refined by: xxx: xxx remove creation date: 1996 To 2010 remove
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1
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
Mortality and incidence in women with 47,XXX and variants
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Mortality and incidence in women with 47,XXX and variants

American journal of medical genetics. Part A, 2010-02, Vol.152A (2), p.367-372 [Peer Reviewed Journal]

Copyright © 2010 Wiley‐Liss, Inc. ;Copyright 2010 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.33214 ;PMID: 20101696

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3
Prenatal diagnosis of 47,XXX
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Prenatal diagnosis of 47,XXX

American journal of obstetrics and gynecology, 2005-05, Vol.192 (5), p.1469 [Peer Reviewed Journal]

ISSN: 0002-9378 ;EISSN: 1097-6868 ;DOI: 10.1016/j.ajog.2004.12.037 ;PMID: 15902140

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4
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome

Journal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Peer Reviewed Journal]

Copyright 2002 Journal of Medical Genetics ;2002 INIST-CNRS ;COPYRIGHT 2002 BMJ Publishing Group Ltd. ;Copyright: 2002 Copyright 2002 Journal of Medical Genetics ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.39.3.217 ;PMID: 11897829 ;CODEN: JMDGAE

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5
Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee
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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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6
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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7
47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development
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47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development

Fertility and sterility, 2009-11, Vol.92 (5), p.1747.e5-1747.e7 [Peer Reviewed Journal]

American Society for Reproductive Medicine ;2009 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2009.07.1008 ;PMID: 19732877

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8
The craniofacial complex in 47, XXX females
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Article
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The craniofacial complex in 47, XXX females

European journal of orthodontics, 2005-08, Vol.27 (4), p.396-401 [Peer Reviewed Journal]

ISSN: 0141-5387 ;EISSN: 1460-2210 ;DOI: 10.1093/ejo/cji016 ;PMID: 16043476 ;CODEN: EJOODK

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9
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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10
Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)
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Root length in the permanent teeth of women with an additional X chromosome (47,XXX females)

Acta odontologica Scandinavica, 2010-07, Vol.68 (4), p.223 [Peer Reviewed Journal]

EISSN: 1502-3850 ;DOI: 10.3109/00016357.2010.490954 ;PMID: 20568965

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11
Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX
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Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX

Birth defects research. A Clinical and molecular teratology, 2007-08, Vol.79 (8), p.612-613 [Peer Reviewed Journal]

Copyright © 2007 Wiley‐Liss, Inc. ;2007 Wiley-Liss, Inc. ;ISSN: 1542-0752 ;EISSN: 1542-0760 ;DOI: 10.1002/bdra.20371 ;PMID: 17469201

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12
Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX Mosaicism
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Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX Mosaicism

Internal Medicine, 2009, Vol.48(6), pp.447-453 [Peer Reviewed Journal]

2009 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.48.1157 ;PMID: 19293545

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13
Kallmann syndrome in a 47,XXX patient
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Kallmann syndrome in a 47,XXX patient

American journal of medical genetics. Part A, 2005-11, Vol.139A (1), p.52-53 [Peer Reviewed Journal]

Copyright © 2005 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.30996 ;PMID: 16222664

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14
Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases
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Double trisomy 48,XXX,+18 in association with increased nuchal translucency; two cases

Prenatal diagnosis, 2004-12, Vol.24 (12), p.1020-1021 [Peer Reviewed Journal]

Copyright © 2004 John Wiley & Sons, Ltd. ;ISSN: 0197-3851 ;EISSN: 1097-0223 ;DOI: 10.1002/pd.1047 ;PMID: 15614873

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15
Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature
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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 Literature

Fetal 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. ;ISSN: 1015-3837 ;EISSN: 1421-9964 ;DOI: 10.1159/000284929 ;PMID: 20160426

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16
Thoracic imaging case presented at the General Case Reading Session of the XXX National Congress of the SERAM, A Coruña. May 2010
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Thoracic imaging case presented at the General Case Reading Session of the XXX National Congress of the SERAM, A Coruña. May 2010

Radiologia, 2010-11, Vol.52 (6), p.567 [Peer Reviewed Journal]

EISSN: 1578-178X ;DOI: 10.1016/j.rx.2010.08.004 ;PMID: 20947108

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17
Musculoskeletal imaging case presented at the General Case Reading Session of the XXX National Congress of the Spanish Society of Diagnostic Imaging (SERAM), A Coruña. May 2010
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Musculoskeletal imaging case presented at the General Case Reading Session of the XXX National Congress of the Spanish Society of Diagnostic Imaging (SERAM), A Coruña. May 2010

Radiologia, 2010-11, Vol.52 (6), p.560 [Peer Reviewed Journal]

EISSN: 1578-178X ;DOI: 10.1016/j.rx.2010.08.001 ;PMID: 20950832

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18
A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotype
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A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotype

Endokrynologia polska, 2010-03, Vol.61 (2), p.217-219 [Peer Reviewed Journal]

2010. This work is published under https://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: 0423-104X ;PMID: 20464710

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19
Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXX
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Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXX

Journal of the American Academy of Child and Adolescent Psychiatry, 1998-03, Vol.37 (3), p.286-291 [Peer Reviewed Journal]

1998 The American Academy of Child and Adolescent Psychiatry ;1998 INIST-CNRS ;Copyright Lippincott Williams & Wilkins Mar 1998 ;ISSN: 0890-8567 ;EISSN: 1527-5418 ;DOI: 10.1097/00004583-199803000-00013 ;PMID: 9519633 ;CODEN: JAAPEE

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20
Female-to-male transsexual with 47,XXX karyotype
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Female-to-male transsexual with 47,XXX karyotype

Biological 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: BIPCBF

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