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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
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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
Sex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXX
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Sex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXX

Endocrine Connections, 2023-08, Vol.12 (9), p.1-10 [Peer Reviewed Journal]

the author(s) ;the author(s) 2023 the author(s) ;ISSN: 2049-3614 ;EISSN: 2049-3614 ;DOI: 10.1530/EC-22-0440 ;PMID: 37399523

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3
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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4
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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5
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
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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7
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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8
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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9
Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanoma
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Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanoma

British journal of cancer, 2007-07, Vol.97 (2), p.223-230 [Peer Reviewed Journal]

ISSN: 0007-0920 ;EISSN: 1532-1827 ;DOI: 10.1038/sj.bjc.6603839 ;PMID: 17595666

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10
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

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11
Differential Expression of VEGF-A^sub xxx^ Isoforms Is Critical for Development of Pulmonary Fibrosis
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Differential Expression of VEGF-A^sub xxx^ Isoforms Is Critical for Development of Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2017-08, Vol.196 (4), p.479 [Peer Reviewed Journal]

Copyright American Thoracic Society Aug 15, 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970 ;DOI: 10.1164/rccm.201603-0568OC

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12
Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient
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Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient

Stem cell research, 2017-08, Vol.23 (C), p.57-60 [Peer Reviewed Journal]

2017 ;Copyright © 2017. Published by Elsevier B.V. ;ISSN: 1873-5061 ;EISSN: 1876-7753 ;DOI: 10.1016/j.scr.2017.06.002 ;PMID: 28925367

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13
Premature ovarian failure related to trisomy X: Two case reports with an aberrant 47, XXX karyotype
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Premature ovarian failure related to trisomy X: Two case reports with an aberrant 47, XXX karyotype

Journal of human reproductive sciences, 2021-01, Vol.14 (1), p.87-90 [Peer Reviewed Journal]

COPYRIGHT 2021 Indian Society of Assisted Reproduction ;COPYRIGHT 2021 Medknow Publications and Media Pvt. Ltd. ;2021. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright: © 2021 Journal of Human Reproductive Sciences 2021 ;ISSN: 0974-1208 ;EISSN: 1998-4766 ;DOI: 10.4103/jhrs.JHRS_59_20 ;PMID: 34083998

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14
Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature
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Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature

Molecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00732-n/a [Peer Reviewed Journal]

2019 The Authors. published by Wiley Periodicals, Inc. ;2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. ;Copyright John Wiley & Sons, Inc. Jul 2019 ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.732 ;PMID: 31070017

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15
A Rare Karyotype of Turner Syndrome: 45.X/47.XXX/Nadir Gorulen Bir Turner Sendromu Karyotipi: 45,X/47,XXX
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A Rare Karyotype of Turner Syndrome: 45.X/47.XXX/Nadir Gorulen Bir Turner Sendromu Karyotipi: 45,X/47,XXX

Güncel pediatri, 2014-04, Vol.12 (1), p.43 [Peer Reviewed Journal]

COPYRIGHT 2014 Galenos Yayinevi Tic. Ltd. ;ISSN: 1304-9054 ;DOI: 10.4274/jcp.02996

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16
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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17
A Rare Karyotype of Turner Syndrome: 45.X/47.XXX
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A Rare Karyotype of Turner Syndrome: 45.X/47.XXX

Güncel pediatri, 2014-04, Vol.12 (1), p.43-47 [Peer Reviewed Journal]

ISSN: 1304-9054 ;EISSN: 1308-6308 ;DOI: 10.4274/jcp.02996

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18
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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19
Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18
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Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18

Case reports in pathology, 2018-01, Vol.2018, p.2839765-5 [Peer Reviewed Journal]

Copyright © 2018 Sujal I. Shah et al. ;COPYRIGHT 2018 Hindawi Limited ;Copyright © 2018 Sujal I. Shah et al. 2018 ;ISSN: 2090-6781 ;EISSN: 2090-679X ;DOI: 10.1155/2018/2839765 ;PMID: 29707399

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20
Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus
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Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetus

Archives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Peer Reviewed Journal]

Springer-Verlag Berlin Heidelberg 2013 ;Archives of Gynecology and Obstetrics is a copyright of Springer, (2013). All Rights Reserved. ;ISSN: 0932-0067 ;EISSN: 1432-0711 ;DOI: 10.1007/s00404-013-2847-3 ;PMID: 23625330

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