ROSSI, ELENA

ROSSI, ELENA  

DIPARTIMENTO DI MEDICINA MOLECOLARE  

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A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea. 1-gen-2008 Rossi, Elena; A. P., Verri; M. G., Patricelli; V., Destefani; I., Ricca; Vetro, Annalisa; Ciccone, Roberto; R., Giorda; D., Toniolo; P., Maraschio; Zuffardi, Orsetta
13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients. 1-gen-2007 L., Ballarati; Rossi, Elena; Mt, Bonati; S., Gimelli; P., Maraschio; P., Finelli; S., Giglio; E., Lapi; Mf, Bedeschi; S., Guerneri; G., Arrigo; Mg, Patricelli; T., Mattina; O., Guzzardi; V., Pecile; A., Police; G., Scarano; L., Larizza; Zuffardi, Orsetta; D., Giardino
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. 1-gen-2012 S., Gana; Veggiotti, Pierangelo; G., Sciacca; C., Fedeli; A., Bersano; G., Micieli; M., Maghnie; Ciccone, Roberto; Rossi, Elena; K., Plunkett; W., Bi; V. R., Sutton; Zuffardi, Orsetta
8.5 Mb deletion at distal 5p in a male ascertained for azoospermia. 1-gen-2005 Rossi, Elena; DE GREGORI, M.; GRAZIA PATRICELLI, M.; Pramparo, T.; Argentiero, L.; Giglio, S.; Sosta, K.; Foresti, G.; Zuffardi, Orsetta
A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea. 1-gen-2008 Rossi, Elena; Verri, Ap; Patricelli, Mg; Destefani, V; Ricca, Ivana; Vetro, Annalisa; Ciccone, Roberto; Giorda, R; Toniolo, D; Maraschio, Paola; Zuffardi, Orsetta
A newborn with ambiguous genitalia and a complex X;Y rearrangement. 1-gen-2014 Dehghani, M; Rossi, Elena; Vetro, Annalisa; Russo, G; Hashemian, Z; Zuffardi, Orsetta
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
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.
Alazami syndrome: Phenotypic expansion and clinical resemblance to Smith–Lemli–Opitz syndrome 1-gen-2020 Gana, S.; Plumari, M.; Rossi, E.; Saracino, A.; Iorio, M.; Zanaboni, M. P.; Orcesi, S.; Valente, E. M.
Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR). 1-gen-2002 Meloni, I; Vitelli, F; Pucci, L; Lowry, Rb; Tonlorenzi, R; Rossi, Elena; Ventura, M; Rizzoni, G; Kashtan, Ce; Pober, B; Renieri, A.
Analysis of XX SRY-negative sex reversal dogs 1-gen-2020 Albarella, Sara; De Lorenzi, Lisa; Rossi, Elena; Prisco, Francesco; Georgia Riccardi, Marita; Restucci, Brunella; Ciotola, Francesca; Parma, Pietro
Case of Myhre syndrome with autism and peculiar skin histological findings. 1-gen-2001 Titomanlio, L; Marzano, Mg; Rossi, Elena; D'Armiento, M; DE BRASI, D; Vega, Gr; Andreucci, Mv; Orsini, Av; Santoro, L; Sebastio, G.
Centromere Repositioning in Cattle (Bos taurus) Chromosome 17 1-gen-2017 De Lorenzi, Lisa; Iannuzzi, Alessandra; Rossi, Elena; Bonacina, Stefania; Parma, Pietro
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.
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome). 1-gen-2009 Coldren, Cd; Lai, Z; Shragg, P; Rossi, Elena; Glidewell, Sc; Zuffardi, Orsetta; Mattina, T; Ivy, Dd; Curfs, Lm; Mattson, Sn; Riley, Ep; Treier, M; Grossfeld, Pd
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature. 1-gen-2006 Rizzolio, F; Bione, S; Sala, C; Goegan, M; Gentile, M; Gregato, Giuliana; Rossi, Elena; Pramparo, Tiziano; Zuffardi, Orsetta; Toniolo, D.
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.
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. 1-gen-2008 Koolen, Da; Sharp, Aj; Hurst, Ja; Firth, Hv; Knight, Sj; Goldenberg, A; SAUGIER VEBER, P; Pfundt, R; Vissers, Le; Destrée, A; Grisart, B; Rooms, L; VAN DER AA, N; Field, M; Hackett, A; Bell, K; Nowaczyk, Mj; Mancini, Gm; Poddighe, Pj; Schwartz, Ce; Rossi, Elena; DE GREGORI, Manuela; ANTONACCI FULTON, Ll; MCLELLAN MD, Nd; Garrett, Jm; Wiechert, Ma; Miner, Tl; Crosby, S; Ciccone, Roberto; Willatt, L; Rauch, A; Zenker, M; Aradhya, S; Manning, Ma; Strom, Tm; Wagenstaller, J; KREPISCHI SANTOS, Ac; VIANNA MORGANTE, Am; Rosenberg, C; Price, Sm; Stewart, H; SHAW SMITH, C; Brunner, Hg; Wilkie, Ao; Veltman, Ja; Zuffardi, Orsetta; Eichler, Ee; DE VRIES, Bb
Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidases 1-gen-1999 Monti, E.; Preti, A.; Rossi, Elena; Ballabio, A.; Borsani, G.
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