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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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Characterization and evolutionary implications of the triad Asp-Xxx-Glu in group II phosphopantetheinyl transferasesWang, Yue-Yue ; Li, Yu-Dong ; Liu, Jian-Bo ; Ran, Xin-Xin ; Guo, Yuan-Yang ; Ren, Ni-Ni ; Chen, Xin ; Jiang, Hui ; Li, Yong-Quan Jeltsch, AlbertPloS one, 2014-07, Vol.9 (7), p.e103031-e103031 [Periódico revisado por pares]United States: Public Library of ScienceTexto 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 |
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Material Type: Artigo
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Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYYAhlawat, Nivedita ; Elliott, Kathryn ; Ormond, Kelly E. ; Allyse, Megan A. ; Riggan, Kirsten A.Journal of community genetics, 2024-02, Vol.15 (1), p.75-83 [Periódico revisado por pares]Berlin/Heidelberg: Springer Berlin HeidelbergTexto completo disponível |
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Material Type: Artigo
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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reportsSugawara, Nobuo ; Maeda, Machiko ; Manome, Tomomi ; Nagai, Rie ; Araki, YasuhisaReproductive medicine and biology, 2013-10, Vol.12 (4), p.193-195 [Periódico revisado por pares]Tokyo: Springer JapanTexto completo disponível |
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Material Type: Artigo
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Sonnet XXX: Love, Dignity, and DyingEly, E. WesleyThe Linacre quarterly, 2016-05, Vol.83 (2), p.150-156 [Periódico revisado por pares]Los Angeles, CA: SAGE PublicationsTexto completo disponível |
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Material Type: Artigo
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The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidyTartaglia, Nicole ; Howell, Susan ; Wilson, Rebecca ; Janusz, Jennifer ; Boada, Richard ; Martin, Sydney ; Frazier, Jacqueline B ; Pfeiffer, Michelle ; Regan, Karen ; McSwegin, Sarah ; Zeitler, PhilipJournal of multidisciplinary healthcare, 2015, Vol.8 (default), p.323-334 [Periódico revisado por pares]New Zealand: Dove Medical Press LimitedTexto completo disponível |
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Material Type: Artigo
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Incidence of sex chromosome aneuploidy in a prenatal population: 27‐year longitudinal study in Northern ItalySamango‐Sprouse, C. A. ; Grati, F. R. ; Brooks, M. ; Hamzik, M. P. ; Khaksari, K. ; Gropman, A. ; Taylor, A. ; Malvestiti, F. ; Grimi, B. ; Liuti, R. ; Milani, S. ; Chinetti, S. ; Trotta, A. ; Agrati, C. ; Repetti, E. ; Martin, K. A.Ultrasound in obstetrics & gynecology, 2023-08, Vol.62 (2), p.266-272 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Triple X syndrome with rare phenotypic presentationJagadeesh, Sujatha ; Jabeen, Gazala ; Bhat, Lathaa ; Vasikarla, Madhavi ; Suresh, Arvind ; Seshadri, Suresh ; Lata, S.Indian journal of pediatrics, 2008-06, Vol.75 (6), p.629-631 [Periódico revisado por pares]India: Springer-VerlagTexto completo disponível |
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Material Type: Artigo
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Supplement.3 XII Congress - XXX Annual Meeting. Rosario Biology Society. ROSARIO, SANTA FE - ARGENTINABiocell, 2011-01, Vol.35, p.153Mendoza: Tech Science PressTexto completo disponível |