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Acrofacial dysostosis of Nager and ocular abnormalities.
Pavone L, Mollica F, Pero G, Tigano G, Giancarlo H, Mattucci K, Setzen M. Pavone L, et al. Among authors: mollica f. Ophthalmic Paediatr Genet. 1986 Aug;7(2):115-9. doi: 10.3109/13816818609076119. Ophthalmic Paediatr Genet. 1986. PMID: 3097597
New syndrome: exostoses, anetodermia, brachydactyly.
Mollica F, Li Volti S, Guarneri B. Mollica F, et al. Am J Med Genet. 1984 Dec;19(4):665-7. doi: 10.1002/ajmg.1320190406. Am J Med Genet. 1984. PMID: 6334993 No abstract available.
The fragile X in Sicily: an epidemiological survey.
Neri G, Sanfilippo S, Pavone L, Mollica F, Barberi I, Giuffrè L, Romano C, Mattina T, Cammarata M, Ragusa MG, et al. Neri G, et al. Among authors: mollica f. Am J Med Genet. 1988 May-Jun;30(1-2):665-72. doi: 10.1002/ajmg.1320300167. Am J Med Genet. 1988. PMID: 3177477
Hereditary twenty-nail dystrophy in a Sicilian family.
Pavone L, Li Volti S, Guarneri B, La Rosa M, Sorge G, Incorpora G, Mollica F. Pavone L, et al. Among authors: mollica f. J Med Genet. 1982 Oct;19(5):337-40. doi: 10.1136/jmg.19.5.337. J Med Genet. 1982. PMID: 7143386 Free PMC article.
Familial congenital brachial palsy.
Mollica F, Li Volti S, Grasso A, De Simone D. Mollica F, et al. Am J Med Genet. 1991 Dec 1;41(3):322-4. doi: 10.1002/ajmg.1320410312. Am J Med Genet. 1991. PMID: 1789287
191 results