Positional cloning of the Fanconi anaemia group A gene von Jansen, Stander, Easton, Douglas F, Memeo, Elena, Deaven, Larry L, D'Apolito, Maria, Pronk, Jan C, Cleton-Jansen, Anne-Marie, Verlander, Peter C, Batish, Sat Dev, Mathew, Christopher G, Notarangeio, Angelo, Cornelisse, Cees J, Moyzis, Robert K, Auerbach, Arleen D, Lennon, Gregory, lanzano, Leonarda, Whitmore, Scott A, Callen, David F, Sutherland, Grant R, Doggett, Norman A, Savino, Maria, Apostolou, Sinoula, Morgan, Neil V, de Ravel, Thomy J, Gibson, Rachel A, Crawford, Joanna, Zelante, Leopoldo, Tipping, Alex J, Moerland, Elna W, Levran, Orna, Savoia, Anna, Van Berkell, Carola, Piemontese, Maria Rosaria, Hassock, Sheila, Erlich, Tamar

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Two newborns with chromosome 4 imbalances : deletion 4q33→q35 and ring r(4)(pterq35.2-qter) von CALABRESE, G, GIANNOTTI, A, MINGARELLI, R, DI GILIO, M. C, PIEMONTESE, M. R, PALKA, G

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Detection of dystrophin deletion carriers using FISH analysis von Calvano, S., Memeo, E., Piemontese, M. R., Melchionda, S., Bisceglia, L., Gasparini, P., Zelante, L.

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The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study von Neri, M, Rossi, R, Trabanelli, C, Mauro, A, Selvatici, R, Falzarano, MS, Spedicato, N, Margutti, A, Rimessi, P, Fortunato, F, Fabris, M, Gualandi, F, Comi, G, Tedeschi, S, Seia, M, Fiorillo, C, Traverso, M, Bruno, C, Giardina, E, Piemontese, MR, Merla, G, Cau, M, Marica, M, Scuderi, C, Borgione, E, Tessa, A, Astrea, G, Santorelli, FM, Merlini, L, Mora, M, Bernasconi, P, Gibertini, S, Sansone, V, Mongini, T, Berardinelli, A, Pini, A, Liguori, R, Filosto, M, Messina, S, Vita, G, Toscano, A, Pane, M, Servidei, S, Pegoraro, E, Bello, L, Travaglini, L, Bertini, E, D'Amico, A, Ergoli, M, Politano, L, Torella, A, Nigro, V, Mercuri, E, Ferlini, A

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Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene von SAVOIA, A, PIEMONTESE, M. R, ZELANTE, L, SAVINO, M, ZATTERALE, A, PRONK, J, ARWERT, F, JOENJE, H, RAMENGHI, U, DANGA-BRICARELLI, F, DALLAPICCOLA, B

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A YAC Contig Spanning the Blepharophimosis-Ptosis- Epicanthus inversus Syndrome and Propionic Acidemia Loci von Piemontese, Maria Rosaria, Memeo, Elena, Carella, Massimo, Amati, Patrizia, Chomel, Jean-Claude, Bonneau, Dominique, Pilia, Giuseppe, Cao, Antonio, Drabkin, Harry, Gemmili, Robert, Rommens, Johanna, Zelante, Leopoldo, Casparini, Paolo, Bisceglia, Luigi

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Linkage analysis in two large Italian pedigrees affected with nail patella syndrome von Melchionda, S, Seri, M, Carella, M, Piemontese, M R, Zhang, X X, Zelante, L, Romeo, G, Gasparini, P

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Cellular Retinol Binding Protein 1 (RBP1): A frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome gene von Bisceglia, L, d»Ambrosio, L, Piemontese, M.R, Carella, M, Amati, P, Bonneau, D, Pilia, G, Gasparini, P, Zelante, L

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Two 48,XXYY patients: clinical, cytogenetic and molecular aspects von Zelante, L, Piemontese, M.R, Francioli, G, Calvano, S

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