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Vol. 52. Núm. 5.
Páginas 483-484 (mayo 2000)
Acceso a texto completo
Un caso de síndrome de Klinefelter 48 XXYY
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O. Vall Combellesa, F. Soléb, M. Bonet Alcainaa, E. Lloverasb, O. García Algara,*
a Servicio de Pediatría. Hospital del Mar. Barcelona.
b Laboratorio de Citología Hematológica. Laboratorio de Referencia de Cataluña. Hospital del Mar. Barcelona.
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Bibliografía
[1.]
H-R. Wiedemann, J. Kunze.
Clinical syndromes, 3.a,
[2.]
KL. Jones.
W.B. Saunders Company, (1997),
[3.]
SB. Friedman, MM. Fisher, BK. Schonberg, EM. Alderman.
Comprehensive adolescent health care, 2.a,
[4.]
CM. Smyth, WJ. Bremner.
Klinefelter syndrome.
Arch Intern Med, 158 (1998), pp. 1309-1314
[5.]
R. King, J. Rotter, A. Motulsky.
Oxford University Press, (1992),
[6.]
JJ. Barbería, FJ. Lafita, EL. Menéndez, RM. Rodríguez.
Descripción clínica y evaluación hormonal de un varón 48, XXYY. Comparación con los casos previos publicados.
Rev Med Univ Navarra, 34 (1990), pp. 97-99
[7.]
R. Franco-Vicario, M. Molina, P. Martínez-Olaizola, JA. Castaños, F. Miguel.
Síndrome de Klinefelter 48 XXYY.
An Med Interna, 7 (1990), pp. 107-108
[8.]
H. Neugebauer, E. Steichen-Gersdorf, J. Glatzl.
Penoscrotale Hypospadie mit XXYY-Chromosomensatz.
Padiatr Padol, 26 (1991), pp. 43-46
Copyright © 2000. Asociación Española de Pediatría
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