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Results: 1-5 |
Results: 5

Authors: Bassi, MT Bergen, AAB Bitoun, P Charles, SJ Clementi, M Gosselin, R Hurst, J Lewis, RA Lorenz, B Meitinger, T Messiaen, L Ramesar, RS Ballabio, A Schiaffino, MV
Citation: Mt. Bassi et al., Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America, HUM GENET, 108(1), 2001, pp. 51-54

Authors: d'Addio, M Pizzigoni, A Bassi, MT Baschirotto, C Valetti, C Incerti, B Clementi, M De Luca, M Ballabio, A Schiaffino, MV
Citation: M. D'Addio et al., Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1, HUM MOL GEN, 9(20), 2000, pp. 3011-3018

Authors: Incerti, B Cortese, K Pizzigoni, A Surace, EM Varani, S Coppola, M Jeffery, G Seeliger, M Jaissle, G Bennett, DC Marigo, V Schiaffino, MV Tacchetti, C Ballabio, A
Citation: B. Incerti et al., Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1, HUM MOL GEN, 9(19), 2000, pp. 2781-2788

Authors: Schiaffino, MV d'Addio, M Alloni, A Baschirotto, C Valetti, C Cortese, K Puri, C Bassi, MT Colla, C De Luca, M Tacchetti, C Ballabio, A
Citation: Mv. Schiaffino et al., Ocular albinism: evidence for a defect in an intracellular signal transduction system, NAT GENET, 23(1), 1999, pp. 108-112

Authors: Burns, WN Schiaffino, MV Lewis, RA
Citation: Wn. Burns et al., Repeated transmission of X-linked ocular albinism type 1 by a carrier oocyte donor, FERT STERIL, 70(6), 1998, pp. 1169-1172
Risultati: 1-5 |