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Familial schizencephaly associated with EMX2 mutation.
Granata T, Farina L, Faiella A, Cardini R, D'Incerti L, Boncinelli E, Battaglia G. Granata T, et al. Among authors: faiella a. Neurology. 1997 May;48(5):1403-6. doi: 10.1212/wnl.48.5.1403. Neurology. 1997. PMID: 9153481
Schizencephaly: surgical features and new molecular genetic results.
Capra V, De Marco P, Moroni A, Faiella A, Brunelli S, Tortori-Donati P, Andreussi I, Boncinelli E, Cama A. Capra V, et al. Among authors: faiella a. Eur J Pediatr Surg. 1996 Dec;6 Suppl 1:27-9. doi: 10.1055/s-2008-1071034. Eur J Pediatr Surg. 1996. PMID: 9008816
Linkage mapping of Emx2 to mouse chromosome 19.
Bosetti A, Faiella A, Boncinelli E, Consalez GG. Bosetti A, et al. Among authors: faiella a. Mamm Genome. 1997 Jan;8(1):71-2. doi: 10.1007/s003359900356. Mamm Genome. 1997. PMID: 9021159 No abstract available.
Homeobox genes and cancer.
Cillo C, Faiella A, Cantile M, Boncinelli E. Cillo C, et al. Among authors: faiella a. Exp Cell Res. 1999 Apr 10;248(1):1-9. doi: 10.1006/excr.1999.4451. Exp Cell Res. 1999. PMID: 10094807 Review.
BgIII RFLP at the HOX1I locus.
Faiella A, Migliaccio E, Boncinelli E. Faiella A, et al. Nucleic Acids Res. 1990 Oct 25;18(20):6179. doi: 10.1093/nar/18.20.6179-a. Nucleic Acids Res. 1990. PMID: 1978297 Free PMC article.
Homeobox genes in normal and malignant cells.
Cillo C, Cantile M, Faiella A, Boncinelli E. Cillo C, et al. Among authors: faiella a. J Cell Physiol. 2001 Aug;188(2):161-9. doi: 10.1002/jcp.1115. J Cell Physiol. 2001. PMID: 11424082 Review.
88 results