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Page 1
X chromosome monosomy: a common mechanism for autoimmune diseases.
Invernizzi P, Miozzo M, Selmi C, Persani L, Battezzati PM, Zuin M, Lucchi S, Meroni PL, Marasini B, Zeni S, Watnik M, Grati FR, Simoni G, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: miozzo m. J Immunol. 2005 Jul 1;175(1):575-8. doi: 10.4049/jimmunol.175.1.575. J Immunol. 2005. PMID: 15972694
Frequency of monosomy X in women with primary biliary cirrhosis.
Invernizzi P, Miozzo M, Battezzati PM, Bianchi I, Grati FR, Simoni G, Selmi C, Watnik M, Gershwin ME, Podda M. Invernizzi P, et al. Among authors: miozzo m. Lancet. 2004 Feb 14;363(9408):533-5. doi: 10.1016/S0140-6736(04)15541-4. Lancet. 2004. PMID: 14975617
Primary biliary cirrhosis: does X mark the spot?
Selmi C, Invernizzi P, Miozzo M, Podda M, Gershwin ME. Selmi C, et al. Among authors: miozzo m. Autoimmun Rev. 2004 Nov;3(7-8):493-9. doi: 10.1016/j.autrev.2004.05.003. Autoimmun Rev. 2004. PMID: 15546796 Review.
Three cases with de novo 6q imbalance and variable prenatal phenotype.
Grati FR, Lalatta F, Turolla L, Cavallari U, Gentilin B, Rossella F, Cetin I, Antonazzo P, Bellotti M, Dulcetti F, Baldo D, Tenconi R, Simoni G, Miozzo M. Grati FR, et al. Among authors: miozzo m. Am J Med Genet A. 2005 Jul 30;136(3):254-8. doi: 10.1002/ajmg.a.30837. Am J Med Genet A. 2005. PMID: 15957159
233 results