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Mapping a dominant form of multinodular goiter to chromosome Xp22.
Capon F, Tacconelli A, Giardina E, Sciacchitano S, Bruno R, Tassi V, Trischitta V, Filetti S, Dallapiccola B, Novelli G. Capon F, et al. Among authors: novelli g. Am J Hum Genet. 2000 Oct;67(4):1004-7. doi: 10.1086/303095. Epub 2000 Sep 11. Am J Hum Genet. 2000. PMID: 10986044 Free PMC article.
Advances in the search for psoriasis susceptibility genes.
Capon F, Dallapiccola B, Novelli G. Capon F, et al. Among authors: novelli g. Mol Genet Metab. 2000 Sep-Oct;71(1-2):250-5. doi: 10.1006/mgme.2000.3031. Mol Genet Metab. 2000. PMID: 11001818 Review.
Association study of a promoter polymorphism of UFD1L gene with schizophrenia.
De Luca A, Pasini A, Amati F, Botta A, Spalletta G, Alimenti S, Caccamo F, Conti E, Trakalo J, Macciardi F, Dallapiccola B, Novelli G. De Luca A, et al. Among authors: novelli g. Am J Med Genet. 2001 Aug 8;105(6):529-33. doi: 10.1002/ajmg.1489. Am J Med Genet. 2001. PMID: 11496370
Role of genetics in prevention of coronary atherosclerosis.
Novelli G, Borgiani P, Giardina E, Mango R, Contino G, Romeo F, Mehta JL. Novelli G, et al. Curr Opin Cardiol. 2003 Sep;18(5):368-71. doi: 10.1097/00001573-200309000-00008. Curr Opin Cardiol. 2003. PMID: 12960469 Review.
1,183 results