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Bibliografía
[1.]
H. Angelman.
Puppet children: A report on three cases.
Rev Med Child Neurol, 7 (1965), pp. 681-688
[2.]
C.A. Williams, R.T. Zori, J. Hendrickson, H. Stalker, T. Marum, E. Whidden, D.J. Driscoll.
Angelman Syndrome.
Curr Prob Pediatr, 25 (1995), pp. 216-231
[3.]
J. Campos-Castelló, G. Bueno-Lozano, M.T. De Santos-Moreno.
El fenómeno del imprinting genómico y sus implicaciones en clínica neuropediátrica.
Rev Neurol, 28 (1999), pp. 69-73
[4.]
R.T. Zori, J. Hendrickson, S. Woolven, E.M. Whidden, B. Cray, C.A. Williams.
Angelman syndrome:clinical profile.
J Child Neurol, 7 (1992), pp. 279-280
[5.]
I.M. Buntix, R.C.M. Ilunnekam, O.F. Brower, H. Stroink, J. Beuten, K. Mangelsehots, J.P. Fryns.
Clinical profile of Angelman syndrome ad different ages.
Am J Med Genet, 56 (1995), pp. 176-183
[6.]
A. Smith, C. Wiles, E. Haan, J. Mc Gill, G. Wallace, J. Dixon, et al.
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.
J Med Genet, 33 (1996), pp. 107-112
[7.]
J. Clayton-Smith.
Clinical research on Angelman syndrome in the United Kingdom: Observations on 82 affected individuals.
Am J Med Genet, 46 (1993), pp. 12-15
[8.]
L.A. Laan, W.O. Renier, W.K. Arts, I.M. Buntinx, I.J. Vd Burgt, H. Stroink, et al.
Evolution of epilepsy and EEG findings in Angelman syndrome.
Epilepsia, 38 (1997), pp. 195-199
[9.]
M. Moreno García, E. Barreiro Miranda.
Síndromes de microdelección: Prader-Willi y Angelman.
Acta Pediatr Esp, 57 (1999), pp. 300-308
[10.]
S. Russo, F. Cogliat, M. Viri, F. Cavalleri, A. Salicorni, L. Turolla, et al.
Novel mutation of ubiquitin protein ligase 3A gene in Italian patients with Angelman síndrome.
Hum Mutat Online, 15 (2000), pp. 387
[11.]
A. Moncla, P. Malzac, M.A. Voelckel, P. Auquier, L. Cirardot, M.G. Mattei, et al.
Phenotype-genotype correlation in 20 deletion and non-deletion Angelman syndrome patients.
Eur J Hum Genet, 7 (1999), pp. 131-139
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