Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Article
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case reportMedicine (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: 36316845Full text available |
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2 |
Material Type: Article
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic WomanInternal 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: 24694497Full text available |
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3 |
Material Type: Article
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Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctationFertility and sterility, 2008-06, Vol.89 (6), p.1826.e5-1826.e7 [Peer Reviewed Journal]American Society for Reproductive Medicine ;2008 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2007.06.065 ;PMID: 17953951Full text available |
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4 |
Material Type: Article
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47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal developmentFertility and sterility, 2009-11, Vol.92 (5), p.1747.e5-1747.e7 [Peer Reviewed Journal]American Society for Reproductive Medicine ;2009 American Society for Reproductive Medicine ;ISSN: 0015-0282 ;EISSN: 1556-5653 ;DOI: 10.1016/j.fertnstert.2009.07.1008 ;PMID: 19732877Full text available |
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5 |
Material Type: Article
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Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX MosaicismInternal 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: 19293545Full text available |
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6 |
Material Type: Article
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Doctors’ experiences of adverse events in secondary care: the professional and personal impactClinical 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: 25468840Full text available |
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7 |
Material Type: Article
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Neurofibromatosis complicated with XXX syndrome and renovascular hypertensionJournal 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: 8656147Full text available |
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8 |
Material Type: Article
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XXX 18-TRISOMYThe Lancet (British edition), 1963-12, Vol.2 (7320), p.1276-1277 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 14066862Full text available |
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9 |
Material Type: Article
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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: 30864638Full text available |
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10 |
Material Type: Article
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XXX 21-trisomy and retinoblastomaThe Lancet (British edition), 1963-07, Vol.2 (7299), p.154-155 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 14025631Full text available |
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11 |
Material Type: Article
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Antenatal diagnosis of an XXX female. A dilemma for genetic counselingThe Western journal of medicine, 1975-07, Vol.123 (1), p.17-21 [Peer Reviewed Journal]ISSN: 0093-0415 ;EISSN: 1476-2978 ;PMID: 1154778Full text available |
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12 |
Material Type: Article
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XXY son of a possibly XX-XXX motherThe Lancet (British edition), 1972-03, Vol.1 (7752), p.697-698 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4125211Full text available |
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13 |
Material Type: Article
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XXY son of XX-XXX motherThe Lancet (British edition), 1972-04, Vol.1 (7757), p.955-955 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4112113Full text available |
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14 |
Material Type: Article
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Plasma factor-VIII concentrations in XXX womenThe Lancet (British edition), 1971-01, Vol.1 (7689), p.58-59 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4099216Full text available |
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15 |
Material Type: Article
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The XXX syndrome frequency among mental defectives and fertilityThe Lancet (British edition), 1960-09, Vol.2 (7151), p.626-627 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 13701513Full text available |
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16 |
Material Type: Article
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XO-XX-XXX mosaicism with Turner stigmataThe Lancet (British edition), 1967-06, Vol.1 (7501), p.1228-1229 [Peer Reviewed Journal]ISSN: 0140-6736 ;EISSN: 1474-547X ;PMID: 4165148Full text available |
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17 |
Material Type: Article
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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 reportMedicine (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: 32702826Full text available |
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18 |
Material Type: Article
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Chromosomal abnormalities detected by karyotyping among patients with secondary amenorrhea: a retrospective studySão 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: 37042862Full text available |
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19 |
Material Type: Article
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Analysis of 17,428 pregnant women undergoing non-invasive prenatal testing for fetal chromosome in Northeast ChinaMedicine (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: 33578623Full text available |
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20 |
Material Type: Article
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Over-expression of XIST, the Master Gene for X Chromosome Inactivation, in Females With Major Affective DisordersEBioMedicine, 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: 26425698Full text available |