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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: Dataset
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Material Type: Dataset
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Material Type: Dataset
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Material Type: Artigo
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Gene Delivery to Joints by Intra-Articular InjectionEvans, Christopher H ; Ghivizzani, Steven C ; Robbins, Paul DHuman gene therapy, 2018-01, Vol.29 (1), p.2-14 [Periódico revisado por pares]United States: Mary Ann Liebert, IncTexto completo disponível |
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Material Type: Artigo
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Validation of an Objective Assessment Tool for Tonsillectomy in Otolaryngology Resident TrainingJakubowski, Luke ; Leader, Brittany A. ; Ishman, Stacey L. ; Chun, Robert ; Tarima, Sergey S. ; Parikh, Sanjay ; Skinner, Margaret ; Thorne, Marc ; Weatherly, Robert ; Wiet, Gregory ; Brown, David J.The Laryngoscope, 2021-02, Vol.131 (2), p.E359-E366 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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X chromosome aneuploidies and schizophrenia: association analysis and phenotypic characterizationKushima, Itaru ; Aleksic, Branko ; Kimura, Hiroki ; Nakatochi, Masahiro ; Lo, Tzuyao ; Ikeda, Masashi ; Arai, Makoto ; Hashimoto, Ryota ; Numata, Shusuke ; Okamura, Yasunobu ; Obara, Taku ; Inada, Toshiya ; Ozaki, NorioPsychiatry and clinical neurosciences, 2022-12, Vol.76 (12), p.667-673 [Periódico revisado por pares]Melbourne: John Wiley & Sons Australia, 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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Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospitalYao, H. ; Jiang, F. ; Hu, H. ; Gao, Y. ; Zhu, Z. ; Zhang, H. ; Wang, Y. ; Guo, Y. ; Liu, L. ; Yuan, Y. ; Zhou, L. ; Wang, J. ; Du, B. ; Qu, N. ; Zhang, R. ; Dong, Y. ; Xu, H. ; Chen, F. ; Jiang, H. ; Liu, Y. ; Zhang, L. ; Tian, Z. ; Liu, Q. ; Zhang, C. ; Pan, X. ; Yang, S. ; Zhao, L. ; Wang, W. ; Liang, Z.Ultrasound in obstetrics & gynecology, 2014-07, Vol.44 (1), p.17-24 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Livro
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Mount Sinai expert guides: Allergy and clinical immunologySampson, Hugh AWILEY 2015Texto completo disponível |