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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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Preparation and fabrication of a full‐scale, sagittal‐sliced, 3D‐printed, patient‐specific radiotherapy phantomCraft, Daniel F. ; Howell, Rebecca M.Journal of applied clinical medical physics, 2017-09, Vol.18 (5), p.285-292 [Periódico revisado por pares]United States: John Wiley & Sons, IncTexto 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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Assessment of PlanIQ Feasibility DVH for head and neck treatment planningFried, David V. ; Chera, Bhishamjit S. ; Das, Shiva K.Journal of applied clinical medical physics, 2017-09, Vol.18 (5), p.245-250 [Periódico revisado por pares]United States: John Wiley and Sons IncTexto completo disponível |
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Material Type: Artigo
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Parental imprinting on the mouse X chromosome: effects on the early development of X0, XXY and XXX embryosTada, Takashi ; Takagi, Nobuo ; Adler, Ilse-DoreGenetical Research, 1993-10, Vol.62 (2), p.139-148Cambridge, UK: Cambridge University PressTexto completo disponível |
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Material Type: Artigo
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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 reportLi, Xiaozhou ; Ju, Duan ; Shi, Yunfang ; Li, Yan ; Dong, Haiwei ; Huang, Jianhua ; Zhang, YingMedicine (Baltimore), 2020-07, Vol.99 (29), p.e20848-e20848 [Periódico revisado por pares]United States: Wolters Kluwer HealthTexto completo disponível |
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Material Type: Artigo
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Noninvasive prenatal detection of fetal sex chromosome abnormalities using the semiconductor sequencing platform (SSP) in Southern ChinaYang, Jiexia ; Hou, Yaping ; Guo, Fangfang ; Peng, Haishan ; Wang, Dongmei ; Li, Yi ; OY, Haoxin ; Wang, Yixia ; Lu, Jian ; Yin, AihuaJournal of assisted reproduction and genetics, 2021-03, Vol.38 (3), p.727-734 [Periódico revisado por pares]New York: Springer USTexto completo disponível |
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Material Type: Artigo
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The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomesMartel, Rachel A. ; Blakemore, Jennifer K. ; Fino, M. ElizabethJournal of assisted reproduction and genetics, 2022-05, Vol.39 (5), p.1143-1153 [Periódico revisado por pares]New York: Springer USTexto 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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Autism, language and communication in children with sex chromosome trisomiesBishop, Dorothy V M ; Jacobs, Patricia A ; Lachlan, Katherine ; Wellesley, Diana ; Barnicoat, Angela ; Boyd, Patricia A ; Fryer, Alan ; Middlemiss, Prisca ; Smithson, Sarah ; Metcalfe, Kay ; Shears, Deborah ; Leggett, Victoria ; Nation, Kate ; Scerif, GaiaArchives of disease in childhood, 2011-10, Vol.96 (10), p.954-959 [Periódico revisado por pares]London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child HealthTexto completo disponível |