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Page 1
Trisomy 10qter confirmed by in situ hybridisation.
Briscioli V, Floridia G, Rossi E, Selicorni A, Lalatta F, Zuffardi O. Briscioli V, et al. Among authors: selicorni a. J Med Genet. 1993 Jul;30(7):601-3. doi: 10.1136/jmg.30.7.601. J Med Genet. 1993. PMID: 8411036 Free PMC article.
Kaufman oculocerebrofacial syndrome in a girl of 15 years.
Briscioli V, Manoukian S, Selicorni A, Livini E, Lalatta F. Briscioli V, et al. Among authors: selicorni a. Am J Med Genet. 1995 Jul 31;58(1):21-3. doi: 10.1002/ajmg.1320580106. Am J Med Genet. 1995. PMID: 7573151 Review.
FISH analysis in Prader-Willi and Angelman syndrome patients.
Bettio D, Rizzi N, Giardino D, Grugni G, Briscioli V, Selicorni A, Carnevale F, Larizza L. Bettio D, et al. Among authors: selicorni a. Am J Med Genet. 1995 Mar 27;56(2):224-8. doi: 10.1002/ajmg.1320560222. Am J Med Genet. 1995. PMID: 7625450
Variability of the Brachmann-de Lange syndrome.
Selicorni A, Lalatta F, Livini E, Briscioli V, Piguzzi T, Bagozzi DC, Mastroiacovo P, Zampino G, Gaeta G, Pugliese A, et al. Selicorni A, et al. Am J Med Genet. 1993 Nov 15;47(7):977-82. doi: 10.1002/ajmg.1320470708. Am J Med Genet. 1993. PMID: 8291540
[Syndromes in outpatient experience].
Lalatta F, Selicorni A, Briscioli V. Lalatta F, et al. Among authors: selicorni a. Pediatr Med Chir. 1993 May-Jun;15 Suppl 1:60-3. Pediatr Med Chir. 1993. PMID: 8415203 Italian.
Seizure and EEG patterns in Angelman's syndrome.
Viani F, Romeo A, Viri M, Mastrangelo M, Lalatta F, Selicorni A, Gobbi G, Lanzi G, Bettio D, Briscioli V, et al. Viani F, et al. Among authors: selicorni a. J Child Neurol. 1995 Nov;10(6):467-71. doi: 10.1177/088307389501000609. J Child Neurol. 1995. PMID: 8576558
263 results