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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: lalatta f. Am J Med Genet. 1995 Jul 31;58(1):21-3. doi: 10.1002/ajmg.1320580106. Am J Med Genet. 1995. PMID: 7573151 Review.
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. Among authors: lalatta f. Am J Med Genet. 1993 Nov 15;47(7):977-82. doi: 10.1002/ajmg.1320470708. Am J Med Genet. 1993. PMID: 8291540
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: lalatta f. 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.
[Syndromes in outpatient experience].
Lalatta F, Selicorni A, Briscioli V. Lalatta F, et al. Pediatr Med Chir. 1993 May-Jun;15 Suppl 1:60-3. Pediatr Med Chir. 1993. PMID: 8415203 Italian.
The Williams syndrome: an Italian collaborative study.
Franceschini P, Guala A, Vardeu MP, Signorile F, Franceschini D, Mastroiacovo P, Gianotti A, Livini E, Lalatta F, Selicorni A, Andria G, Scarano G, Della Monica M, Rizzo R, Zelante L, Stabile M, Gabrielli O, Neri G. Franceschini P, et al. Among authors: lalatta f. Minerva Pediatr. 1996 Oct;48(10):421-8. Minerva Pediatr. 1996. PMID: 9017917
Malignant melanoma and Charcot-Marie-Tooth disease: a further case.
Manoukian S, Briscioli V, Lalatta F. Manoukian S, et al. Among authors: lalatta f. Am J Med Genet. 1997 Jan 20;68(2):242. doi: 10.1002/(sici)1096-8628(19970120)68:2<242::aid-ajmg25>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9028468 No abstract available.
121 results