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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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Low recurrence rate of hepatocellular carcinoma after liver transplantation: Better patient selection or lower immunosuppression?VIVARELLI, M ; BELLUSCI, R ; CUCCHETTI, A ; CAVRINI, G ; DE RUVO, N ; ADEN, A. A ; LA BARBA, G ; BRILLANTI, S ; CAVALLARI, ATransplantation, 2002-12, Vol.74 (12), p.1664-1665 [Periódico revisado por pares]Hagerstown, MD: LippincottTexto 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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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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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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Material Type: Artigo
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Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18Chen, Chih-Ping ; Chern, Schu-Rern ; Yeh, Li-Fan ; Chen, Wen-Lin ; Chen, Li-Feng ; Wang, WayseenPrenatal diagnosis, 2000-09, Vol.20 (9), p.750-753 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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Trisomy 8 mosaicism in a patient born to a mother with 47,XXXNucaro, Anna Lisa ; Cao, Antonio ; Faedda, Antonella ; Crisponi, GiangiorgioAmerican journal of medical genetics, 2003-05, Vol.119A (1), p.85-86 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Rett syndrome in a 47,XXX patient with a de novo MECP2 mutationHammer, Sara ; Dorrani, Naghmeh ; Hartiala, Jaana ; Stein, Stuart ; Schanen, N. CarolynAmerican journal of medical genetics, 2003-10, Vol.122A (3), p.223-226 [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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Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at pubertyBlair, Joanne ; Tolmie, John ; Hollman, Anne S. ; Donaldson, Malcolm D.C.The Journal of pediatrics, 2001-11, Vol.139 (5), p.724-728 [Periódico revisado por pares]New York, NY: Mosby, IncTexto completo disponível |
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Material Type: Artigo
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Karyotype 69,XXX/47,XX,+15 in a 2 1/2 year old childDean, J ; Cohen, G ; Kemp, J ; Robson, L ; Tembe, V ; Hasselaar, J ; Webster, B ; Lammi, A ; Smith, AJournal of medical genetics, 1997-03, Vol.34 (3), p.246-249 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |