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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: 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.
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
Thomas syndrome: clinical variability and autosomal recessive inheritance.
Briscioli V, Lalatta F, Rizzuti T, Fesslová V. Briscioli V, et al. Among authors: lalatta f. Am J Med Genet. 1997 Aug 22;71(3):373-4. doi: 10.1002/(sici)1096-8628(19970822)71:3<373::aid-ajmg23>3.0.co;2-g. Am J Med Genet. 1997. PMID: 9268113 No abstract available.
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
De Gregori M, Ciccone R, Magini P, Pramparo T, Gimelli S, Messa J, Novara F, Vetro A, Rossi E, Maraschio P, Bonaglia MC, Anichini C, Ferrero GB, Silengo M, Fazzi E, Zatterale A, Fischetto R, Previderé C, Belli S, Turci A, Calabrese G, Bernardi F, Meneghelli E, Riegel M, Rocchi M, Guerneri S, Lalatta F, Zelante L, Romano C, Fichera M, Mattina T, Arrigo G, Zollino M, Giglio S, Lonardo F, Bonfante A, Ferlini A, Cifuentes F, Van Esch H, Backx L, Schinzel A, Vermeesch JR, Zuffardi O. De Gregori M, et al. Among authors: lalatta f. J Med Genet. 2007 Dec;44(12):750-62. doi: 10.1136/jmg.2007.052787. Epub 2007 Aug 31. J Med Genet. 2007. PMID: 17766364 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.
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.
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