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Prenatal diagnosis of 47,XXXKhoury-Collado, Fady ; Wehbeh, Ammar N. ; Fisher, Allan J. ; Bombard, Allan T. ; Weiner, ZeevAmerican journal of obstetrics and gynecology, 2005-05, Vol.192 (5), p.1469-1471 [Periódico revisado por pares]Philadelphia, PA: Mosby, IncTexto completo disponível |
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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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Pharmacological Properties of Traditional Medicine (XXX): Effects of Gyokuheifusan (玉屏風散) on Murine Antigen-Specific Antibody ProductionMakino, Toshiaki ; Sasaki, Shin-ya ; Ito, Yoshiaki ; Kano, YoshihiroBiological and Pharmaceutical Bulletin, 2005, Vol.28(1), pp.110-113 [Periódico revisado por pares]Japan: The Pharmaceutical Society of JapanTexto completo disponível |
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Systemic lupus erythematosus in a multiethnic US Cohort (LUMINA). XXX: association between C-reactive protein (CRP) gene polymorphisms and vascular eventsSzalai, A. J. ; Alarcón, G. S. ; Calvo-Alén, J. ; Toloza, S. M. A. ; McCrory, M. A. ; Edberg, J. C. ; McGwin, G. ; Bastian, H. M. ; Fessler, B. J. ; Vilá, L. M. ; Kimberly, R. P. ; Reveille, J. D.Rheumatology (Oxford, England), 2005-07, Vol.44 (7), p.864-868 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |
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Material Type: Artigo
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The craniofacial complex in 47, XXX femalesKrušinskie, Viktorija ; Alvesalo, Lassi ; Šidlauskas, AntanasEuropean journal of orthodontics, 2005-08, Vol.27 (4), p.396-401 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |
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Partial Epilepsy and 47,XXX Karyotype: Report of Four CasesRoubertie, Agathe ; Humbertclaude, Véronique ; Leydet, Julie ; Lefort, Geneviève ; Echenne, BernardPediatric neurology, 2006-07, Vol.35 (1), p.69-74 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypesPatwardhan, Anil J. ; Brown, Wendy E. ; Bender, Bruce G. ; Linden, Mary G. ; Eliez, Stephan ; Reiss, Allan L.American journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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47,XXX associated with malformationsHaverty, Carrie E. ; Lin, Angela E. ; Simpson, Ellen ; Spence, M. Anne ; Martin, Rick A.American journal of medical genetics, 2004-02, Vol.125A (1), p.108-111 [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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Long survival in a 69,XXX triploid infant in GreeceIliopoulos, Dimitrios ; Vassiliou, Georgia ; Sekerli, Eleni ; Sidiropoulou, Vasiliki ; Tsiga, Alexandra ; Dimopoulou, Despina ; Voyiatzis, NikolaosGenetics and molecular research, 2005-12, Vol.4 (4), p.755-759 [Periódico revisado por pares]BrazilTexto 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 |