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A finding in genetic polymorphism analysis study: A case of non-mosaic 47, XXX without manifestationsYang, Xingyi ; Ye, Zilan ; Zhang, Xiaofang ; Wang, Huijun ; Liu, ChaoLegal medicine (Tokyo, Japan), 2017-07, Vol.27, p.38-42 [Periódico revisado por pares]Ireland: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Hemodynamics During Liver TransplantationCosta, M.G ; Chiarandini, P ; Della Rocca, GTransplantation proceedings, 2007-07, Vol.39 (6), p.1871-1873 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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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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Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctationChen, Chih-Ping, M.D ; Lin, Shuan-Pei, M.D ; Tsai, Fuu-Jen, M.D ; Chern, Schu-Rern, MS ; Wang, Wayseen, MSFertility and sterility, 2008-06, Vol.89 (6), p.1826.e5-1826.e7 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Sirenomelia: a review on embryogenic enviromental theories, novel three-dimensional ultrasound imaging and first trimester diagnosis in a case of mosaic 69,XXX/46,XX fetusGabriele, Tonni ; Gianpaolo, GrisoliaArchives of gynecology and obstetrics, 2013-07, Vol.288 (1), p.3-11 [Periódico revisado por pares]Berlin/Heidelberg: Springer-VerlagTexto 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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Kallmann syndrome in a 47,XXX patientCorssmit, E.P.M. ; Seminara, S.B. ; Pitteloud, N. ; Fliers, E.American journal of medical genetics. Part A, 2005-11, Vol.139A (1), p.52-53 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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HOX gene cluster (de)regulation in brain: from neurodevelopment to malignant glial tumoursGonçalves, Céline S. ; Le Boiteux, Elisa ; Arnaud, Philippe ; Costa, Bruno M.Cellular and molecular life sciences : CMLS, 2020-10, Vol.77 (19), p.3797-3821 [Periódico revisado por pares]Cham: Springer International PublishingTexto completo disponível |
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Material Type: Artigo
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Implications of failure to achieve a result from prenatal maternal serum cell‐free DNA testing: a historical cohort studyChan, N ; Smet, M‐E ; Sandow, R ; Silva Costa, F ; McLennan, ABJOG : an international journal of obstetrics and gynaecology, 2018-06, Vol.125 (7), p.848-855 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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The accuracy of prenatal cell-free DNA screening for sex chromosome abnormalities: A systematic review and meta-analysisBussolaro, Sofia ; Raymond, Yvette C. ; Acreman, Melissa L. ; Guido, Maurizio ; Da Silva Costa, Fabricio ; Rolnik, Daniel L. ; Fantasia, IlariaAmerican journal of obstetrics & gynecology MFM, 2023-03, Vol.5 (3), p.100844, Article 100844 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |