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1
Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndrome
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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2
Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful knee
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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3
Long-term survival in a 69,XXX triploid premature infant
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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4
Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular events
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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5
Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient
Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient
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Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient

American journal of medical genetics. Part A, 2012-01, Vol.158A (1), p.206-214 [Peer Reviewed Journal]

Copyright © 2011 Wiley Periodicals, Inc. ;2015 INIST-CNRS ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.34364 ;PMID: 22106088

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6
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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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7
Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature
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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8
Female-to-male transsexual with 47,XXX karyotype
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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9
Transition From Adolescence to Early Adulthood: Adaptation and Psychiatric Status of Women With 47,XXX
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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10
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
Doctors’ experiences of adverse events in secondary care: the professional and personal impact
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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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11
Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation
Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation
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Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation

American 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: 12966522

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12
Trisomy 8 mosaicism in a patient born to a mother with 47,XXX
Trisomy 8 mosaicism in a patient born to a mother with 47,XXX
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Trisomy 8 mosaicism in a patient born to a mother with 47,XXX

American journal of medical genetics. Part A, 2003-05, Vol.119A (1), p.85-86 [Peer Reviewed Journal]

Copyright © 2003 Wiley‐Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20086 ;PMID: 12707966

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13
Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty
Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty
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Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at puberty

The Journal of pediatrics, 2001-11, Vol.139 (5), p.724-728 [Peer Reviewed Journal]

2001 Mosby, Inc. ;2002 INIST-CNRS ;ISSN: 0022-3476 ;EISSN: 1097-6833 ;DOI: 10.1067/mpd.2001.118571 ;PMID: 11713453 ;CODEN: JOPDAB

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14
Genetics of Childhood Disorders: XXX. Autoimmune Disorders, Part 3: Myasthenia Gravis and Rasmussen's Encephalitis
Genetics of Childhood Disorders: XXX. Autoimmune Disorders, Part 3: Myasthenia Gravis and Rasmussen's Encephalitis
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Genetics of Childhood Disorders: XXX. Autoimmune Disorders, Part 3: Myasthenia Gravis and Rasmussen's Encephalitis

Journal 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: JAAPEE

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15
The parental origin of the extra X chromosome in 47,XXX females
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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16
Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy
Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy
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Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy

Journal of medical genetics, 1993-07, Vol.30 (7), p.597-600 [Peer Reviewed Journal]

1993 INIST-CNRS ;Copyright BMJ Publishing Group LTD Jul 1993 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.30.7.597 ;PMID: 8411035 ;CODEN: JMDGAE

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17
Azoospermia in a 46,xx/47,xxx phenotypic male
Azoospermia in a 46,xx/47,xxx phenotypic male
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Azoospermia in a 46,xx/47,xxx phenotypic male

Urology (Ridgewood, N.J.), 1996-12, Vol.48 (6), p.947-948 [Peer Reviewed Journal]

1996 Elsevier Science Inc. ;1997 INIST-CNRS ;ISSN: 0090-4295 ;EISSN: 1527-9995 ;DOI: 10.1016/S0090-4295(96)00321-4 ;PMID: 8973686 ;CODEN: URGYAZ

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18
Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX
Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX
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Prenatal diagnosis and prognosis of triple X syndrome: 47, XXX

Journal de gynécologie, obstétrique et biologie de la reproduction, 2009-11, Vol.38 (7), p.599-603

2009 Elsevier Masson SAS ;2009 INIST-CNRS ;ISSN: 0368-2315 ;DOI: 10.1016/j.jgyn.2009.08.003 ;PMID: 19762167 ;CODEN: JGOBAC

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19
Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child
Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child
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Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old child

Journal of medical genetics, 1997-03, Vol.34 (3), p.246-249 [Peer Reviewed Journal]

1997 INIST-CNRS ;Copyright BMJ Publishing Group LTD Mar 1997 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg.34.3.246 ;PMID: 9132499 ;CODEN: JMDGAE

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20
Neurofibromatosis complicated with XXX syndrome and renovascular hypertension
Neurofibromatosis complicated with XXX syndrome and renovascular hypertension
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Neurofibromatosis complicated with XXX syndrome and renovascular hypertension

Journal 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: 8656147

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