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1 |
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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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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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndromeSybert, V PJournal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto 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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Yearly Occurrence and Seasonality of Neuro-ophthalmic Manifestations of Pediatric Lyme DiseaseSilverstein, Marlee ; Jordan, Catherine O ; Aylward, Shawn C ; Inger, HilliaryJournal of pediatric ophthalmology and strabismus, 2024-05, Vol.61 (3), p.179-182 [Periódico revisado por pares]United States: Slack, IncTexto completo disponível |
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Material Type: Artigo
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Sports injuries and illnesses during the London Summer Olympic Games 2012Engebretsen, Lars ; Soligard, Torbjørn ; Steffen, Kathrin ; Alonso, Juan Manuel ; Aubry, Mark ; Budgett, Richard ; Dvorak, Jiri ; Jegathesan, Manikavasagam ; Meeuwisse, Willem H ; Mountjoy, Margo ; Palmer-Green, Debbie ; Vanhegan, Ivor ; Renström, Per ABritish journal of sports medicine, 2013-05, Vol.47 (7), p.407-414 [Periódico revisado por pares]England: BMJ Publishing Group Ltd and British Association of Sport and Exercise MedicineTexto completo disponível |
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Material Type: Artigo
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Prenatal Diagnosis of Congenital Diaphragmatic Hernia in a McFadden Kalousek Type 2 Triploid FetusBianca, S. ; Ettore, G. ; Gullotta, G. ; Galasso, M.G.Fetal diagnosis and therapy, 2004-01, Vol.19 (1), p.49-51 [Periódico revisado por pares]Basel, Switzerland: KargerTexto completo disponível |
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Material Type: Artigo
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Atypical Rett syndrome in a girl with mosaic triple X and MECP2 variantTakahashi, Satoru ; Takeguchi, Ryo ; Kuroda, Mami ; Tanaka, RyosukeMolecular genetics & genomic medicine, 2020-03, Vol.8 (3), p.e1122-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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The predictive role of pelvic magnetic resonance in the follow up of spontaneous or induced puberty in turner syndromeMaggio, M C ; De Pietro, A ; Porcelli, P ; Serraino, F ; Angileri, T ; Di Peri, A ; Corsello, GItalian journal of pediatrics, 2018-02, Vol.44 (1), p.24-24, Article 24 [Periódico revisado por pares]England: BioMed CentralTexto completo disponível |
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Material Type: Artigo
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Clinical predictors and management for radial artery spasm: an Australian cross-sectional studyCurtis, Elizabeth ; Fernandez, Ritin ; Khoo, John ; Weaver, James ; Lee, Astin ; Halcomb, LizBMC cardiovascular disorders, 2023-01, Vol.23 (1), p.33-33, Article 33 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |