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22q11.2 deletion syndrome in patients admitted to a cardiac pediatric intensive care unit in BrazilRosa, Rafael F.M. ; Pilla, Carlo B. ; Pereira, Vera L.B. ; Flores, José A.M. ; Golendziner, Eliete ; Koshiyama, Dayane B. ; Hertz, Michele T. ; Ricachinevsky, Cláudia P. ; Roman, Tatiana ; Varella-Garcia, Marileila ; Paskulin, Giorgio A.American journal of medical genetics. Part A, 2008-07, Vol.146A (13), p.1655-1661 [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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25-year experience of using a linear stapler in laryngectomyBedrin, Lev ; Ginsburg, Genadi ; Horowitz, Zeev ; Talmi, Yoav P.Head & neck, 2005-12, Vol.27 (12), p.1073-1079 [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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3D Reconstruction of the Mouse's MesonephrosVazquez, M.-D. ; Bouchet, P. ; Mallet, J.-L. ; Foliguet, B. ; Gérard, H. ; LeHeup, B.Anatomia, histologia, embryologia, 1998-10, Vol.27 (5), p.283-287 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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Material Type: Artigo
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45,X/46,XX/47,XXX phenotypeLebel, Robert Roger ; Elejalde, B. Rafael ; De Elejalde, Maria Mercedes ; Avila, TeresitaPrenatal diagnosis, 1993-12, Vol.13 (12), p.1165-1166 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdSem texto completo |
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Material Type: Artigo
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45,X/47,XXX/47,XX, del(Y)(p?)/46,XX mosaicism causing true hermaphroditismNieto, Karem ; Peña, Rocío ; Palma, Icela ; Dorantes, Luis M. ; Eraña, Luis ; Alvarez, Rebeca ; García‐Cavazos, Ricardo ; Kofman‐Alfaro, Susana ; Queipo, GloriaAmerican journal of medical genetics. Part A, 2004-10, Vol.130A (3), p.311-314 [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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46, X, i(Xq) karyotype in a patient with hypoplastic left heartShah, Ashok ; Fay, John E. ; Ford, Sally ; Holden, Jeanette J. A.Clinical genetics, 1985-08, Vol.28 (2), p.178-179 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdSem texto completo |
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Material Type: Artigo
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46,XY/48,XXY,+8 in a male with clinical and dermatoglyphic features of mosaic trisomy 8 syndromeCasey, Pamela A. ; Clark, Constance E. ; Cowell, Henry R.Clinical genetics, 1981-07, Vol.20 (1), p.60-63 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdSem texto completo |
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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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Material Type: Artigo
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47,XXY Klinefelter syndrome: Clinical characteristics and age-specific recommendations for medical managementAksglaede, Lise ; Link, Katarina ; Giwercman, Aleksander ; Jørgensen, Niels ; Skakkebæk, Niels E ; Juul, AndersAmerican journal of medical genetics. Part C, Seminars in medical genetics, 2013-02, Vol.163C (1), p.55-63Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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48, XXXY Klinefelter syndrome and nail-patella syndrome in the same childJansen, Jette ; Hansen, Erik ; Hobolth, Niels ; Jacobsen, Petrea ; Mikkelsen, MargaretaClinical genetics, 1976-02, Vol.9 (2), p.163-168 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdSem texto completo |