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Material Type: Artigo
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Attention-Deficit Hyperactivity Disorder Symptoms in Children and Adolescents with Sex Chromosome Aneuploidy: XXY, XXX, XYY, and XXYYTARTAGLIA, Nicole R ; AYARI, Natalie ; HUTAFF-LEE, Christa ; BOADA, RichardJournal of developmental and behavioral pediatrics, 2012-05, Vol.33 (4), p.309-318 [Periódico revisado por pares]Hagerstown, MD: Lippincott Williams & WilkinsTexto completo disponível |
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Material Type: Artigo
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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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3 |
Material Type: Artigo
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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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Material Type: Artigo
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Ultrasound imaging for the rheumatologist XXX. Sonographic assessment of the painful kneeMEENAGH, G ; FILIPPUCCI, E ; DELLE SEDIE, A ; IAGNOCCO, A ; SCIRE, C. A ; RIENTE, L ; MONTECUCCO, C ; VALESINI, G ; BOMBARDIERI, S ; GRASSI, WClinical and experimental rheumatology, 2010-11, Vol.28 (6), p.803-805 [Periódico revisado por pares]Pisa: Clinical and Experimental RheumatologyTexto completo disponível |
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Material Type: Artigo
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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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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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7 |
Material Type: Artigo
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Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the LiteratureBağci, Soyhan ; Müller, Andreas ; Franz, Axel ; Heydweiller, Andreas ; Berg, Christoph ; Nöthen, Markus M. ; Bartmann, Peter ; Reutter, HeikoFetal diagnosis and therapy, 2010-03, Vol.27 (2), p.113-117 [Periódico revisado por pares]Basel, Switzerland: KargerTexto completo disponível |
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8 |
Material Type: Artigo
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Female-to-male transsexual with 47,XXX karyotypeTuran, M.Tayfun ; Eşel, Ertuğrul ; Dündar, Munis ; Candemir, Zuhal ; Baştürk, Mustafa ; Sofuoğlu, Seher ; Özkul, YusufBiological psychiatry (1969), 2000-12, Vol.48 (11), p.1116-1117 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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9 |
Material Type: Artigo
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Spontaneous pregnancy in a woman with 45,X/47,XXX mosaicism in both serum and germ cell lines: A case reportEBLEN, Abby C ; NAKAJIMA, Steve TJournal of reproductive medicine, 2003-02, Vol.48 (2), p.121-123 [Periódico revisado por pares]Saint-Louis, MO: ScienceTexto completo disponível |
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10 |
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 |