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Material Type: Artigo
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A review of trisomy X (47,XXX)Tartaglia, Nicole R ; Howell, Susan ; Sutherland, Ashley ; Wilson, Rebecca ; Wilson, LennieOrphanet journal of rare diseases, 2010-05, Vol.5 (1), p.8-8, Article 8 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Material Type: Artigo
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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves' disease and 47, XXX in a woman: A case reportLiang, Dong ; Han, Minmin ; Xu, Linxin ; Ren, Yi ; Zhang, Yi ; Yin, Jianhong ; Yang, Jing ; Liu, YunfengMedicine (Baltimore), 2022-10, Vol.101 (43), p.e31443-e31443 [Periódico revisado por pares]United States: Lippincott Williams & WilkinsTexto completo disponível |
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Material Type: Artigo
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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 studyBerglund, Agnethe ; Viuff, Mette Hansen ; Skakkebæk, Anne ; Chang, Simon ; Stochholm, Kirstine ; Gravholt, Claus HøjbjergOrphanet journal of rare diseases, 2019-01, Vol.14 (1), p.16-16, Article 16 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
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Material Type: Artigo
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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,+21Li, Jin ; Xie, Mingshui ; Wang, Fang ; Ma, Jianhong ; Li, Jiafu ; Chen, Chen ; Li, Zhimin ; Wang, Juan ; Zhang, Yuanzhen ; Li, YirongMolecular genetics & genomic medicine, 2020-08, Vol.8 (8), p.e1279-n/a [Periódico revisado por pares]United States: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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Ovarian reserve evaluation in a woman with 45,X/47,XXX mosaicism: A case report and a review of literatureTang, Ruiyi ; Lin, Lin ; Guo, Zaixin ; Hou, Haiyan ; Yu, QiMolecular genetics & genomic medicine, 2019-07, Vol.7 (7), p.e00732-n/a [Periódico revisado por pares]United States: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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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 patientChen, Yuchang ; Ou, Zhanhui ; Song, Bing ; Xian, Yexing ; Ouyang, Shuming ; Xie, Yuhuan ; Xue, Yanting ; Sun, XiaofangStem cell research, 2017-08, Vol.23 (C), p.57-60 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Phenotypic variability in 47, XXX patients: Clinical report of four new casesGoldschmidt, Ernesto ; Márquez, Marisa ; Solari, Andrea ; Ziembar, María I ; Laudicina, AlejandroArchivos argentinos de pediatría, 2010-08, Vol.108 (4), p.e88-e91 [Periódico revisado por pares]ArgentinaTexto completo disponível |
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Material Type: Artigo
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Double trisomy with 48, XXX+21 karyotype in a Down’s syndrome child from Jammu and Kashmir, IndiaBalwan, Wahied Khawar ; Kumar, Parvinder ; Raina, T. R. ; Gupta, SubashJournal of genetics, 2008-12, Vol.87 (3), p.257-259 [Periódico revisado por pares]India: Springer-VerlagTexto completo disponível |
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Material Type: Artigo
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A case of premature ovarian failure (POF) in a 31-year-old woman with a 47,XXX karyotypeSkałba, Piotr ; Cygal, Anna ; Gierzyńska, ZuzannaEndokrynologia polska, 2010-03, Vol.61 (2), p.217-219 [Periódico revisado por pares]Poland: Wydawnictwo Via MedicaTexto completo disponível |
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Material Type: Artigo
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Doctors’ experiences of adverse events in secondary care: the professional and personal impactHarrison, Reema ; Lawton, Rebecca ; Stewart, KevinClinical medicine (London, England), 2014-12, Vol.14 (6), p.585-590 [Periódico revisado por pares]London: Elsevier LtdTexto completo disponível |