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Titolo Data di pubblicazione Autore(i) File
DiGeorge anomaly associated with 10p deletion. 1-gen-1991 Monaco, G; Pignata, C; Rossi, Elena; Mascellaro, O; Cocozza, S; Ciccimarra, F.
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. 1-gen-1993 Rossi, Elena; Floridia, G; Casali, M; Danesino, Cesare; Chiumello, G; Bernardi, F; Magnani, I; Papi, L; Mura, M; Zuffardi, Orsetta
Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3-q22.1 1-gen-1993 Rossi, Elena; Zarrilli, R; Zuffardi, Orsetta
Trisomy 10qter confirmed by in siyu hybridization 1-gen-1993 Briscioli, V; Floridia, G; Rossi, Elena; Selicorni, A; Lalatta, F; Zuffardi, Orsetta
D8S7 is consistently deleted in inverted duplication of the short arm of chromosome 8 ( inv dup 8p) 1-gen-1993 Minelli, Antonella; G., Floridia; Rossi, Elena; M., Clementi; R., Tencon; L., Camurri; F., Bernardi
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2 1-gen-1994 Pezzolo, A; Gimelli, G; Sposito, M; Giusani, U; Rossi, Elena; Zuffardi, Orsetta
Molecular cloning of cDNA encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1 1-gen-1994 Corti, O; Finochiaro, G; Rossi, Elena; Zuffardi, Orsetta; Di Donato, S.
order of six loci at 2q24-q31 and orientation of the HOXD locus 1-gen-1994 Rossi, Elena; Faiella, A; Zeviani, M; Labeit, S; Floridia, G; Brunelli, S; Cammarata, M; Boncinelli, E; Zuffardi, Orsetta
Activation of the galectin-1 (L-14-I) gene from nonexpressing differentiated cells by fusion with undifferentiated and tumorigenic cells. 1-gen-1994 Chiariotti, L; Benvenuto, G; Zarrilli, R; Rossi, Elena; Salvatore, P; Colantuoni, V; Bruni, C. B.
The gene (NFE2L1) for human NRF-1, an activator involved in nuclear mitochondrial interaction, maps to 7q32 1-gen-1995 Tiranti, V; Rossi, Elena; Rocchi, M; Di Donato, S; Zuffardi, Orsetta; Zeviani, M.
Colocalization of (TTAGGG)n telomeric sequences and ribosomal genes in Atlantic eels. 1-gen-1995 Salvadori, S; Deiana, Am; Coluccia, E; Floridia, G; Rossi, Elena; Zuffardi, Orsetta
Chromosomal localization of mitochondrial transcription factr A (TCF6), single-straned DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis 1-gen-1995 Tiranti, V; Rossi, Elena; Ruiz carrillo, A; Rossi, G; Rocchi, M; Di Donato, S; Zuffardi, Orsetta; Zeviani, M.
A novel mechnaism for the origin of supernumerary marker chromosomes 1-gen-1996 Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications 1-gen-1996 Floridia, G.; Piantanida, M.; Minelli, Antonella; Dellavecchia, C.; Bonaglia, C.; Rossi, Elena; Gimelli, G.; Croci, G.; Franchi, F.; Gilgenkrantz, S.; Grammatico, P.; Dalpra', L.; Wood, S.; Danesino, Cesare; Zuffardi, Orsetta
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching 1-gen-1996 Banfi, S.; Borsani, G.; Rossi, Elena; Bernard, L.; Guffanti, A.; Rubboli, F.; Marchitiello, A.; Giglio, S.; Coluccia, E.; Zollo, M.; Zuffardi, Orsetta; Ballabio, A.
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein. 1-gen-1996 Nigro, V; Piluso, G; Belsito, A; Politano, L; Puca, Aa; Papparella, S; Rossi, Elena; Viglietto, G; Esposito, Mg; Abbondanza, C; Medici, N; Molinari, Am; Nigro, G; Puca, G. A.
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(x)(pter-->q24::q21.32-->qter) and random X inactivation 1-gen-1997 Carrozzo, R; Arrigo, G; Rossi, Elena; Bardoni, B; Cammarata, M; Gandullia, P; Gatti, R; Zuffardi, Orsetta
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome 1-gen-1997 Carrozzo, R.; Rossi, Elena; Christian, S. L.; Kittikamron, K.; Livieri, C.; Corrias, A.; Pucci, L.; Fois, A.; Simi, P.; Bosio, L.; Beccaria, L.; Zuffardi, Orsetta; Ledbetter, D. H.
A novel zinc finger-containing RNA-binding protein conserved from fruitflies to humans. 1-gen-1997 Jackson, Fr; Banfi, S; Guffanti, A; Rossi, Elena
Chromosome 20 ring: a chromosomal disorder associated with a particular electroclinical pattern. 1-gen-1998 Canevini, Mp; Sgro, V; Zuffardi, Orsetta; Canger, R; Carrozzo, R; Rossi, Elena; Ledbetter, D; Minicucci, F; Vignoli, A; Piazzini, A; Guidolin, L; Saltarelli, A; DALLA BERNARDINA, B.
Mostrati risultati da 1 a 20 di 84
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