Información del artículo
El Texto completo está disponible en PDF
Bibliografía
[1.]
D.C. Aronson, M.C.E. Jansweijer, J.M.N. Hoovers, P.G. Barth.
A male infant with holoprosencephaly associated with ring chromosome 21.
Clin Genet, 31 (1987), pp. 48-52
[2.]
A. Kleczkowska, J.P. Fryns.
Ring chromosome 21 in a normal female.
Ann Genet, 27 (1984), pp. 126-128
[3.]
J.L. Huret, C. Leonard, V. Kanoui.
Ring chromosome in a phenotypically normal but infertile man.
Clin Genet, 28 (1985), pp. 541-545
[4.]
S. Ohga, F. Nakao, O. Narazaki, T. Aoki, K. Kamesaki, T. Hara.
Hypogammaglobulinaemia in a patient with ring chromosome 21.
Arch Dis Child, 77 (1997), pp. 252-255
[5.]
W. Schmid, R. Tenconi, C. Baccichetti, D. Caudin, A. Schinzel.
Ring chromosome 21 in phenotypically apparently normal persons: Reports of two families from Switzerland and Italy.
Am J Med Genet, 16 (1983), pp. 323-329
[6.]
W. Demyer, W. Zeman, C.G. Palmer.
The face predicts the brain: Diagnostic significance of median facial anomalies for holoprosencephaly (arhinencephaly).
Pediatrics, 34 (1964), pp. 256-263
[7.]
E. Niedermeyer, F. Lopes.
Electroencephalography.
Basic principles, clinical applications and related fields, 3rd ed, pp. 510-515
Copyright © 2004. Asociación Española de Pediatría
