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Results: 1-5 |
Results: 5

Authors: Genuardi, M Tozzi, C Pomponi, MG Stagni, ML Della Monica, M Scarano, G Calvieri, F Torrisi, L Neri, G
Citation: M. Genuardi et al., Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies, EUR J HUM G, 7(4), 1999, pp. 421-426

Authors: Chiurazzi, P Pomponi, MG Pietrobono, R Bakker, CE Neri, G Oostra, BA
Citation: P. Chiurazzi et al., Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene, HUM MOL GEN, 8(12), 1999, pp. 2317-2323

Authors: Grasso, M Faravelli, F Lo Nigro, C Chiurazzi, P Sperandeo, MP Argusti, A Pomponi, MG Lecora, M Sebastio, GF Perroni, L Andria, G Neri, G Bricarelli, FD
Citation: M. Grasso et al., Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients, AM J MED G, 85(3), 1999, pp. 311-316

Authors: Chiurazzi, P Pomponi, MG Sharrock, A Macpherson, J Lormeau, S Morel, ML Rousseau, F
Citation: P. Chiurazzi et al., DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature, AM J MED G, 83(4), 1999, pp. 347-349

Authors: Genuardi, M Pomponi, MG Torrisi, L Neri, G Stagni, ML Tozzi, C
Citation: M. Genuardi et al., 45,X/47,XX,+18 constitutional mosaicism: clinical presentation and evidence for a somatic origin of the aneuploid cell lines, J MED GENET, 36(6), 1999, pp. 496-498
Risultati: 1-5 |