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Results: 1-8 |
Results: 8
Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains
Authors: Miano, MG Testa, F Filippini, F Trujillo, M Conte, I Lanzara, C Millan, JM De Bernardo, C Grammatico, B Mangino, M Torrente, I Carrozzo, R Simonelli, F Rinaldi, E Ventruto, V D'Urso, M Ayuso, C Ciccodicola, A
Citation: Mg. Miano et al., Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains, HUM MUTAT, 18(2), 2001, pp. 109-119
Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa
Authors: Vervoort, R Lennon, A Bird, AC Tulloch, B Axton, R Miano, MG Meindl, A Meitinger, T Ciccodicola, A Wright, AF
Citation: R. Vervoort et al., Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa, NAT GENET, 25(4), 2000, pp. 462-466
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region
Authors: Ciccodicola, A D'Esposito, M Esposito, T Gianfrancesco, F Migliaccio, C Miano, MG Matarazzo, MR Vacca, M Franze, A Cuccurese, M Cocchia, M Curci, A Terracciano, A Torino, A Cocchia, S Mercadante, G Pannone, E Archidiacono, N Rocchi, M Schlessinger, D D'Urso, M
Citation: A. Ciccodicola et al., Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region, HUM MOL GEN, 9(3), 2000, pp. 395-401
The highly malignant phenotype of anaplastic thyroid carcinoma cell lines is recessive
Authors: Martelli, ML Miano, MG Battaglia, C Trapasso, F Stella, A Iuliano, R Visconti, R Fagin, JA Santoro, M Fusco, A
Citation: Ml. Martelli et al., The highly malignant phenotype of anaplastic thyroid carcinoma cell lines is recessive, EUR J ENDOC, 143(4), 2000, pp. 515-521
Pitfalls in homozygosity mapping
Authors: Miano, MG Jacobson, SG Carothers, A Hanson, I Teague, P Lovell, J Cideciyan, AV Haider, N Stone, EM Sheffield, VC Wright, AF
Citation: Mg. Miano et al., Pitfalls in homozygosity mapping, AM J HU GEN, 67(5), 2000, pp. 1348-1351
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa
Authors: Miano, MG Testa, F Strazzullo, M Trujillo, M De Bernardo, C Grammatico, B Simonelli, F Mangino, M Torrente, I Ruberto, G Beneyto, M Antinolo, G Rinaldi, E Danesino, C Ventruto, V D'Urso, M Ayuso, C Baiget, M Ciccodicola, A
Citation: Mg. Miano et al., Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa, EUR J HUM G, 7(6), 1999, pp. 687-694
Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family
Authors: Rozzo, C Fossarello, M Galleri, G Miano, MG Ciccodicola, A Sole, G Pirastu, M
Citation: C. Rozzo et al., Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family, EUR J HUM G, 7(5), 1999, pp. 574-578
Human and mouse SYBL1 gene structure and expression
Authors: Matarazzo, MR Cuccurese, M Strazzullo, M Vacca, M Curci, A Miano, MG Cocchia, M Mercadante, G Torino, A D'Urso, M Ciccodicola, A D'Esposito, M
Citation: Mr. Matarazzo et al., Human and mouse SYBL1 gene structure and expression, GENE, 240(1), 1999, pp. 233-238
Risultati: 1-8 |