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European Journal of Biochemistry|February 1, 1993
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chainM Valli, A Sangalli, A Rossi, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 4, 2003
No linkage or association of five polymorphisms in the interleukin-4 receptor alpha gene with atopic asthma in Italian familiesC Migliaccio, C Patuzzo, G Malerba, et al.
Human Genetics|July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen geneM Mottes, A Sangalli, M Valli, et al.
Stem Cell Research & Therapy|April 12, 2025
The bone microenvironment: new insights into the role of stem cells and cell communication in bone regenerationL Dalle Carbonare, M Cominacini, E Trabetti, et al.
Human Mutation|January 1, 1993
Paternal mosaicism for a COL1A1 dominant mutation (alpha 1 Ser-415) causes recurrent osteogenesis imperfectaM Mottes, M M Gomez Lira, M Valli, et al.
Annales De Genetique|January 1, 1992
Cystic fibrosis gene mutations and linked RFLPs in the Slovenian populationM Ravnik-Glavac, P Gasparini, B Peterlin, et al.
Clinical and Experimental Medicine|January 12, 2008
ApoE epsilon2/epsilon3/epsilon4 polymorphism, ApoC-III/ApoE ratio and metabolic syndromeO Olivieri, N Martinelli, A Bassi, et al.
International Journal of Immunogenetics|March 22, 2007
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease riskS Mazzola, M Gomez Lira, M D Benedetti, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|January 21, 2000
Candidate genes and a genome-wide search in Italian families with atopic asthmatic childrenG Malerba, E Trabetti, C Patuzzo, et al.
American Journal of Medical Genetics|October 16, 1996
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 GeneS Rossetti, E Bresin, G Restagno, et al.
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