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1
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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2
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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3
Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies
Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies
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Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies

Cytogenetic and genome research, 2019-01, Vol.159 (3), p.137-142 [Peer Reviewed Journal]

2019 S. Karger AG, Basel ;2019 S. Karger AG, Basel. ;ISSN: 1424-8581 ;EISSN: 1424-859X ;DOI: 10.1159/000504238 ;PMID: 31786569

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4
Double trisomy 48,XXX,+18 with multiple dysmorphic features
Double trisomy 48,XXX,+18 with multiple dysmorphic features
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Double trisomy 48,XXX,+18 with multiple dysmorphic features

World journal of pediatrics : WJP, 2015-02, Vol.11 (1), p.83 [Peer Reviewed Journal]

EISSN: 1867-0687 ;DOI: 10.1007/s12519-015-0005-7 ;PMID: 25822702

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5
Mortality and incidence in women with 47,XXX and variants
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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6
Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX
Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX
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Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47,XXX/46,XX

The journal of obstetrics and gynaecology research, 2014-01, Vol.40 (1), p.259-262 [Peer Reviewed Journal]

2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology ;2013 The Authors. Journal of Obstetrics and Gynaecology Research © 2013 Japan Society of Obstetrics and Gynecology. ;ISSN: 1341-8076 ;EISSN: 1447-0756 ;DOI: 10.1111/jog.12131 ;PMID: 23937348

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7
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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8
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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9
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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10
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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11
Duodenal atresia in an infant with triple‐X syndrome: A new associated malformation in 47,XXX
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
Long survival in a 69,XXX triploid infant in Greece
Long survival in a 69,XXX triploid infant in Greece
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Long survival in a 69,XXX triploid infant in Greece

Genetics and molecular research, 2005-12, Vol.4 (4), p.755-759 [Peer Reviewed Journal]

ISSN: 1676-5680 ;EISSN: 1676-5680 ;PMID: 16475122

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13
A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention
A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention
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A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention

Clinical genetics, 2020-01, Vol.97 (1), p.156 [Peer Reviewed Journal]

2019 The Authors. Clinical Genetics published by John Wiley & Sons Ltd. ;EISSN: 1399-0004 ;DOI: 10.1111/cge.13586 ;PMID: 31267526

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14
Phenotypic variability in 47, XXX patients: Clinical report of four new cases
Phenotypic variability in 47, XXX patients: Clinical report of four new cases
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Phenotypic variability in 47, XXX patients: Clinical report of four new cases

Archivos argentinos de pediatría, 2010-08, Vol.108 (4), p.e88-e91 [Peer Reviewed Journal]

EISSN: 1668-3501 ;DOI: 10.1590/S0325-00752010000400012 ;PMID: 20672182

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15
Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India
Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, India

Journal of genetics, 2008-12, Vol.87 (3), p.257-259 [Peer Reviewed Journal]

Indian Academy of Sciences 2008 ;ISSN: 0022-1333 ;EISSN: 0973-7731 ;DOI: 10.1007/s12041-008-0039-x ;PMID: 19147910

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16
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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17
XXX syndrome
XXX syndrome
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XXX syndrome

Nihon rinshō, 2006-06, Vol.Suppl 2, p.522

ISSN: 0047-1852 ;PMID: 16817456

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18
47,XXX: what is the prognosis?
47,XXX: what is the prognosis?
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47,XXX: what is the prognosis?

Pediatrics (Evanston), 1988-10, Vol.82 (4), p.619-630 [Peer Reviewed Journal]

ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.82.4.619 ;PMID: 2459656

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19
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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20
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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