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1
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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2
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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3
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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4
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21
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A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21

Molecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Peer Reviewed Journal]

2020 The Authors. published by Wiley Periodicals LLC ;2020 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2020. This work is published under http://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: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1279 ;PMID: 32463164

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5
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries

Clinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Peer Reviewed Journal]

2019 The Authors. published by John Wiley & Sons Ltd. ;2019. 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: 2050-0904 ;EISSN: 2050-0904 ;DOI: 10.1002/ccr3.2207 ;PMID: 31183102

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6
LP-105 Synergistic effect of extra X chromosome in the development of systemic lupus erythematosus in klinefelter syndrome karyotype 47, XXY and karyotype 47, XXX females
LP-105 Synergistic effect of extra X chromosome in the development of systemic lupus erythematosus in klinefelter syndrome karyotype 47, XXY and karyotype 47, XXX females
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LP-105 Synergistic effect of extra X chromosome in the development of systemic lupus erythematosus in klinefelter syndrome karyotype 47, XXY and karyotype 47, XXX females

Lupus science & medicine, 2023-07, Vol.10 (Suppl 1), p.A127-A127 [Peer Reviewed Journal]

2023 Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;EISSN: 2053-8790 ;DOI: 10.1136/lupus-2023-KCR.207

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7
Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literature
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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8
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX
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Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX

Genes, 2021-06, Vol.12 (6), p.798 [Peer Reviewed Journal]

2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2073-4425 ;EISSN: 2073-4425 ;DOI: 10.3390/genes12060798 ;PMID: 34073864

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9
Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient
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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10
Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reports
Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reports
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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reports

Reproductive medicine and biology, 2013-10, Vol.12 (4), p.193-195 [Peer Reviewed Journal]

Japan Society for Reproductive Medicine 2013 ;The Japan Society for Reproductive Medicine ;Copyright John Wiley & Sons, Inc. Oct 2013 ;ISSN: 1445-5781 ;EISSN: 1447-0578 ;DOI: 10.1007/s12522-013-0158-9 ;PMID: 29699146

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11
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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12
A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotype
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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13
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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14
The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations
The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations
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The evolutionary history of Drosophila buzzatii. XXX. Mitochondrial DNA polymorphism in original and colonizing populations

Molecular biology and evolution, 1996-02, Vol.13 (2), p.314-323 [Peer Reviewed Journal]

ISSN: 0737-4038 ;EISSN: 1537-1719 ;DOI: 10.1093/oxfordjournals.molbev.a025591 ;PMID: 8587497

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15
Relationship between surgical time and postoperative complications in senile patients with hip fractures
Relationship between surgical time and postoperative complications in senile patients with hip fractures
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Relationship between surgical time and postoperative complications in senile patients with hip fractures

Chinese journal of traumatology, 2010-06, Vol.13 (3), p.167-172 [Peer Reviewed Journal]

2010 The Editorial Board of Biomedical and Environmental Sciences ;Copyright © Wanfang Data Co. Ltd. All Rights Reserved. ;ISSN: 1008-1275 ;DOI: 10.3760/cma.j.issn.1008-1275.2010.03.007 ;PMID: 20515595

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16
Is the effect of melatonin on vascular endothelial growth factor receptor-2 associated with angiogenesis in the rat ovary?
Is the effect of melatonin on vascular endothelial growth factor receptor-2 associated with angiogenesis in the rat ovary?
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Is the effect of melatonin on vascular endothelial growth factor receptor-2 associated with angiogenesis in the rat ovary?

Clinics (São Paulo, Brazil), 2019-01, Vol.74, p.e658-e658, Article e658 [Peer Reviewed Journal]

2019 CLINICS ;This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1807-5932 ;ISSN: 1980-5322 ;EISSN: 1980-5322 ;DOI: 10.6061/clinics/2019/e658 ;PMID: 30864638

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17
Purine N-oxides. XXX. Biochemical studies of the oncogen 3-hydroxyxanthine
Purine N-oxides. XXX. Biochemical studies of the oncogen 3-hydroxyxanthine
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Purine N-oxides. XXX. Biochemical studies of the oncogen 3-hydroxyxanthine

The Journal of biological chemistry, 1969-08, Vol.244 (15), p.4072 [Peer Reviewed Journal]

ISSN: 0021-9258 ;EISSN: 1083-351X ;PMID: 5800434

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18
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
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Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

PloS one, 2016-08, Vol.11 (8), p.e0161045-e0161045 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Samango-Sprouse et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Samango-Sprouse et al 2016 Samango-Sprouse et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0161045 ;PMID: 27512996

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19
Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report
Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report
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Fetal aneuploidy screening by non-invasive prenatal testing of maternal plasma DNA sequencing with "false negative" result due to confined placental mosaicism: A case report

Medicine (Baltimore), 2020-07, Vol.99 (29), p.e20848-e20848 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020848 ;PMID: 32702826

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20
Chromosomal abnormalities detected by karyotyping among patients with secondary amenorrhea: a retrospective study
Chromosomal abnormalities detected by karyotyping among patients with secondary amenorrhea: a retrospective study
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Chromosomal abnormalities detected by karyotyping among patients with secondary amenorrhea: a retrospective study

São Paulo medical journal, 2023, Vol.141 (5), p.e2022426-e2022426 [Peer Reviewed Journal]

This work is licensed under a Creative Commons Attribution 4.0 International License. ;ISSN: 1516-3180 ;ISSN: 1806-9460 ;EISSN: 1806-9460 ;DOI: 10.1590/1516-3180.2022.0426.R1.14012023 ;PMID: 37042862

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