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Results: 1-8 |
Results: 8
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic archdefects in mice
Authors: Lindsay, EA Vitelli, F Su, H Morishima, M Huynh, T Pramparo, T Jurecic, V Ogunrinu, G Sutherland, HF Scambler, PJ Bradley, A Baldini, A
Citation: Ea. Lindsay et al., Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic archdefects in mice, NATURE, 410(6824), 2001, pp. 97-101
Preserved speech variant is allelic of classic Rett syndrome
Authors: De Bona, C Zappella, M Hayek, G Meloni, I Vitelli, F Bruttini, M Cusano, R Loffredo, P Longo, I Renieri, A
Citation: C. De Bona et al., Preserved speech variant is allelic of classic Rett syndrome, EUR J HUM G, 8(5), 2000, pp. 325-330
Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3
Authors: Vitelli, F Meloni, I Fineschi, S Favara, F Storlazzi, CT Rocchi, M Renieri, A
Citation: F. Vitelli et al., Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3, CYTOG C GEN, 88(3-4), 2000, pp. 259-263
Mosaicism in Alport syndrome and genetic counselling
Authors: Bruttini, M Vitelli, F Meloni, I Rizzari, C Della Volpe, M Mazzucco, G De Marchi, M Renieri, A
Citation: M. Bruttini et al., Mosaicism in Alport syndrome and genetic counselling, J MED GENET, 37(9), 2000, pp. 717-719
The Neapolitan gliommero, 'Licinio se 'l mio insegno'
Authors: Vitelli, F
Citation: F. Vitelli, The Neapolitan gliommero, 'Licinio se 'l mio insegno', G STOR LET, 177(577), 2000, pp. 154-155
KCNE1-like gene is deleted in AMME contiguous gene syndrome: Identification and characterization of the human and mouse homologs
Authors: Piccini, M Vitelli, F Seri, M Galietta, LJV Moran, O Bulfone, A Banfi, S Pober, B Renieri, A
Citation: M. Piccini et al., KCNE1-like gene is deleted in AMME contiguous gene syndrome: Identification and characterization of the human and mouse homologs, GENOMICS, 60(3), 1999, pp. 251-257
Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME)
Authors: Vitelli, F Piccini, M Caroli, F Franco, B Malandrini, A Pober, B Jonsson, O Sorrentino, V Renieri, A
Citation: F. Vitelli et al., Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME), GENOMICS, 55(3), 1999, pp. 335-340
Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeralmuscular dystrophy
Authors: Vitelli, F Villanova, M Malandrini, A Bruttini, M Piccini, M Merlini, L Guazzi, G Renieri, A
Citation: F. Vitelli et al., Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeralmuscular dystrophy, MUSCLE NERV, 22(10), 1999, pp. 1437-1441
Risultati: 1-8 |