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1
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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2
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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3
Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic Woman

Internal Medicine, 2014, Vol.53(7), pp.783-787 [Peer Reviewed Journal]

2014 by The Japanese Society of Internal Medicine ;ISSN: 0918-2918 ;EISSN: 1349-7235 ;DOI: 10.2169/internalmedicine.53.1325 ;PMID: 24694497

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4
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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5
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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6
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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7
XXX 18-TRISOMY
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XXX 18-TRISOMY

The Lancet (British edition), 1963-12, Vol.2 (7320), p.1276-1277 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 14066862

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8
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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9
XXX 21-trisomy and retinoblastoma
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XXX 21-trisomy and retinoblastoma

The Lancet (British edition), 1963-07, Vol.2 (7299), p.154-155 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 14025631

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10
Antenatal diagnosis of an XXX female. A dilemma for genetic counseling
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Antenatal diagnosis of an XXX female. A dilemma for genetic counseling

The Western journal of medicine, 1975-07, Vol.123 (1), p.17-21 [Peer Reviewed Journal]

ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778

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11
XXY son of a possibly XX-XXX mother
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XXY son of a possibly XX-XXX mother

The Lancet (British edition), 1972-03, Vol.1 (7752), p.697-698 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4125211

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12
XXY son of XX-XXX mother
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XXY son of XX-XXX mother

The Lancet (British edition), 1972-04, Vol.1 (7757), p.955-955 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4112113

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13
Plasma factor-VIII concentrations in XXX women
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Article
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Plasma factor-VIII concentrations in XXX women

The Lancet (British edition), 1971-01, Vol.1 (7689), p.58-59 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4099216

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14
The XXX syndrome frequency among mental defectives and fertility
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The XXX syndrome frequency among mental defectives and fertility

The Lancet (British edition), 1960-09, Vol.2 (7151), p.626-627 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 13701513

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15
XO-XX-XXX mosaicism with Turner stigmata
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XO-XX-XXX mosaicism with Turner stigmata

The Lancet (British edition), 1967-06, Vol.1 (7501), p.1228-1229 [Peer Reviewed Journal]

ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4165148

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16
CLINICAL CALORIMETRY. XXX. METABOLISM IN ERYSIPELAS
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CLINICAL CALORIMETRY. XXX. METABOLISM IN ERYSIPELAS

Archives of internal medicine (1908), 1922-05, Vol.29 (5), p.567-582

ISSN: 0730-188X ;DOI: 10.1001/archinte.1922.00110050014002

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17
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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18
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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19
Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China
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Clinical Application of Noninvasive Prenatal Testing for Sex Chromosome Aneuploidies in Central China

Frontiers in medicine, 2022-01, Vol.8, p.672211-672211 [Peer Reviewed Journal]

Copyright © 2022 Zhao, Dai, Wang, Liu, Zhao and Kong. ;Copyright © 2022 Zhao, Dai, Wang, Liu, Zhao and Kong. 2022 Zhao, Dai, Wang, Liu, Zhao and Kong ;ISSN: 2296-858X ;EISSN: 2296-858X ;DOI: 10.3389/fmed.2021.672211 ;PMID: 35155454

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20
What should we focus on before preimplantation genetic diagnosis/screening?
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What should we focus on before preimplantation genetic diagnosis/screening?

Archives of medical science, 2018-08, Vol.14 (5), p.1119-1124 [Peer Reviewed Journal]

2018. This work is published under http://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright: © 2018 Termedia & Banach 2018 ;ISSN: 1734-1922 ;EISSN: 1896-9151 ;DOI: 10.5114/aoms.2018.72790 ;PMID: 30154896

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