Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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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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2 |
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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3 |
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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4 |
Material Type: Artigo
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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovariesRafique, Munazzah ; AlObaid, Solaiman ; Al‐Jaroudi, DaniaClinical case reports, 2019-06, Vol.7 (6), p.1238-1241 [Periódico revisado por pares]England: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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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 femalesTan, Irene J ; Khandwala, Pushti ; Sen, MitaliLupus science & medicine, 2023-07, Vol.10 (Suppl 1), p.A127-A127 [Periódico revisado por pares]London: BMJ Publishing Group LTDTexto completo disponível |
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Material Type: Artigo
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Autoimmune Myelofibrosis Accompanied by Sjögren's Syndrome in a 47, XXX/46, XX Mosaic WomanTakahashi, TohruInternal Medicine, 2014, Vol.53(7), pp.783-787 [Periódico revisado por pares]Japan: The Japanese Society of Internal MedicineTexto completo disponível |
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7 |
Material Type: Artigo
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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,XXXPandelache, Alison ; Francis, David ; Oertel, Ralph ; Dickson, Rebecca ; Sachdev, Rani ; Ling, Ling ; Gamage, Dinusha ; Godler, David E.Genes, 2021-06, Vol.12 (6), p.798 [Periódico revisado por pares]Basel: MDPI AGTexto completo disponível |
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8 |
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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9 |
Material Type: Artigo
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Acromegaly Accompanied by Turner Syndrome with 47,XXX/45,X/46,XX MosaicismYamazaki, Masanori ; Sato, Ai ; Nishio, Shin-ichi ; Takeda, Teiji ; Miyamoto, Takahide ; Katai, Miyuki ; Hashizume, KiyoshiInternal Medicine, 2009, Vol.48(6), pp.447-453 [Periódico revisado por pares]Japan: The Japanese Society of Internal MedicineTexto completo disponível |
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10 |
Material Type: Artigo
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Long survival in a 69,XXX triploid infant in GreeceIliopoulos, Dimitrios ; Vassiliou, Georgia ; Sekerli, Eleni ; Sidiropoulou, Vasiliki ; Tsiga, Alexandra ; Dimopoulou, Despina ; Voyiatzis, NikolaosGenetics and molecular research, 2005-12, Vol.4 (4), p.755-759 [Periódico revisado por pares]BrazilTexto completo disponível |