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Blood|May 30, 1998
Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interactionD Girelli, S Friso, E Trabetti, et al.
British Journal of Haematology|December 19, 1998
The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelatedC Borgna-Pignatti, A Solinas, C Bombieri, et al.
Minerva Endocrinologica|October 17, 2008
Foot bone mass and analysis of calcium metabolism in diabetic patients affected by severe neuropathyD Barbaro, P Orsini, P Lapi, et al.
Haematologica|March 1, 1997
Early detection of bone marrow engraftment by amplification of hypervariable DNA regionsG Martinelli, E Trabetti, P Farabegoli, et al.
Molecular and Cellular Probes|August 1, 1993
The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphismsE Trabetti, R Galavotti, L Zanini, et al.
Bone Marrow Transplantation|September 1, 1992
Host origin of bone marrow fibroblasts following allogeneic bone marrow transplantation for chronic myeloid leukemiaM A Santucci, E Trabetti, G Martinelli, et al.
Human Heredity|January 1, 1991
Forensic applications of molecular genetic analysis: an Italian collaborative study on paternity testing by the determination of variable number of tandem repeat DNA polymorphismsP Gasparini, P Mandich, G Novelli, et al.
Human Genetics|June 1, 1994
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfectaM Mottes, A Sangalli, M Valli, et al.
Journal of Medical Genetics|May 1, 1993
Molecular genetic diagnosis of autosomal dominant polycystic kidney disease in a newborn with bilateral cystic kidneys detected prenatally and multiple skeletal malformationsA E Turco, E M Padovani, G P Chiaffoni, et al.
The European Respiratory Journal|March 29, 2003
Tumour necrosis factor family genes in a phenotype of COPD associated with emphysemaI Ferrarotti, M Zorzetto, M Beccaria, et al.
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