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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
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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3
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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4
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 Royal College of Physicians 2014 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.14-6-585 ;PMID: 25468840

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5
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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6
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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7
Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals
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Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals

Medical journal of Australia, 1983-11, Vol.2 (11), p.535 [Peer Reviewed Journal]

ISSN: 0025-729X ;EISSN: 1326-5377 ;DOI: 10.5694/j.1326-5377.1983.tb122644.x ;PMID: 6633377

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8
Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals
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Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals

Medical journal of Australia, 1983-07, Vol.2 (1), p.9 [Peer Reviewed Journal]

ISSN: 0025-729X ;EISSN: 1326-5377 ;DOI: 10.5694/j.1326-5377.1983.tb142065.x ;PMID: 6865834

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9
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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10
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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11
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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12
Gonadal dysgenesis in a neonate with 45,X/47,XXX karyotype
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Gonadal dysgenesis in a neonate with 45,X/47,XXX karyotype

Southern medical journal (Birmingham, Ala.), 1980-10, Vol.73 (10), p.1402 [Peer Reviewed Journal]

ISSN: 0038-4348 ;EISSN: 1541-8243 ;DOI: 10.1097/00007611-198010000-00035 ;PMID: 7434061

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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
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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15
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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16
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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17
Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China
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Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast China

Medicine (Baltimore), 2021-02, Vol.100 (6), p.e24740-e24740 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024740 ;PMID: 33578623

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18
Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective Disorders
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Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective Disorders

EBioMedicine, 2015-08, Vol.2 (8), p.909-918 [Peer Reviewed Journal]

2015 The Authors ;2015 The Authors 2015 ;ISSN: 2352-3964 ;EISSN: 2352-3964 ;DOI: 10.1016/j.ebiom.2015.06.012 ;PMID: 26425698

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19
Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature
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Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature

Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 2013-07, Vol.117 (3), p.714 [Peer Reviewed Journal]

ISSN: 0048-7848 ;PMID: 24502039

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20
Breastfeeding in Spain and the factors related to its establishment and maintenance: LAyDI Study (PAPenRed)
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Article
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Breastfeeding in Spain and the factors related to its establishment and maintenance: LAyDI Study (PAPenRed)

Atención primaria, 2024-01, Vol.56 (1), p.102772-102772 [Peer Reviewed Journal]

Copyright © 2023 The Authors. Publicado por Elsevier España, S.L.U. All rights reserved. ;EISSN: 1578-1275 ;DOI: 10.1016/j.aprim.2023.102772 ;PMID: 37741187

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