Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
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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2 |
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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3 |
Material Type: Artigo
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Turner syndrome phenotype with 47,XXX karyotype: Further investigation warranted?Wallerstein, Robert ; Musen, Erica ; McCarrier, Julie ; Aisenberg, Javier ; Chartoff, Amy ; Hutcheon, R. Gordon ; Tepperberg, James ; Pappenhausen, Peter ; Griffin, SharonAmerican journal of medical genetics, 2004-02, Vol.125A (1), p.106-107 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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4 |
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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5 |
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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6 |
Material Type: Artigo
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47,XXX male: A clinical and molecular studyOgata, Tsutomu ; Matsuo, Mari ; Muroya, Koji ; Koyama, Yasuhiro ; Fukutani, KeikoAmerican journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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7 |
Material Type: Artigo
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Psychosocial competence of unselected young adults with sex chromosome abnormalitiesBender, Bruce G. ; Harmon, Robert J. ; Linden, Mary G. ; Bucher-Bartelson, Becki ; Robinson, ArthurAmerican journal of medical genetics, 1999-04, Vol.88 (2), p.200-206 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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8 |
Material Type: Artigo
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Double trisomy (48,XXX, + 18)Tsukahara, M. ; Fukuda, M. ; Furukawa, S. ; Kondoh, O.American journal of medical genetics, 1994-08, Vol.52 (2), p.244-244New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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9 |
Material Type: Artigo
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Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patientsLin, Henry J. ; Ndiforchu, Fombe ; Patell, ShibaniAmerican journal of medical genetics, 1993-03, Vol.45 (6), p.761-763New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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10 |
Material Type: Artigo
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47,XXX t(7;11)(p 11.2;q11.2) and 48,XXXX t(7;11)(p11.2;q11.2) in the same patientBERES, J ; TIMAR, LAmerican journal of medical genetics, 1992-02, Vol.42 (3), p.395-395New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |