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Haematologica|March 1, 1991
Different suppression of Ph1 positive hemopoiesis induced by intensive chemotherapy in lymphoid and myeloid blast crisis of CMLA Guerrasio, G Martinelli, A Ambrosetti, et al.
Journal of Molecular Evolution|December 1, 1995
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulationsB M Ciminelli, F Pompei, P Malaspina, et al.
Molecular and Cellular Probes|June 17, 1999
Two novel missense mutations causing adrenoleukodystrophy in Italian patientsC Perusi, M Gomez-Lira, M Mottes, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney diseaseA E Turco, S Rossetti, E Bresin, et al.
Clinical Genetics|November 1, 1995
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndromeA E Turco, S Rossetti, M O Biasi, et al.
Human Genetics|December 1, 1994
Complete detection of mutations in cystic fibrosis patients of Native American originB Mercier, O Raguénès, X Estivill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 2010
Variants and haplotypes of TCF7L2 are associated with β-cell function in patients with newly diagnosed type 2 diabetes: the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 1S Bonetti, M Trombetta, G Malerba, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|January 18, 2011
Upregulated expression of Toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expressionS Ferronato, M G Lira, S Olivato, et al.
Acta Diabetologica|November 20, 2012
PPARG2 Pro12Ala and ADAMTS9 rs4607103 as "insulin resistance loci" and "insulin secretion loci" in Italian individuals. The GENFIEV study and the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 4M Trombetta, S Bonetti, M L Boselli, et al.
European Journal of Human Genetics : EJHG|December 7, 2000
Recommendations for quality improvement in genetic testing for cystic fibrosis. European Concerted Action on Cystic FibrosisE Dequeker, H Cuppens, J Dodge, et al.
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