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Molecular and Cellular Probes|December 1, 1996
A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1)E Bresin, S Rossetti, S Englisch, et al.
International Journal of Immunogenetics|November 16, 2007
Two new highly polymorphic markers in the 3' UTR region of the PLA2G7 geneM Gomez Lira, L Provezza, C Terranova, et al.
Molecular and Cellular Probes|March 17, 1998
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A geneC Perusi, M Gomez-Lira, M Mottes, et al.
Headache|March 31, 2001
Frequency of factor V Leiden in juvenile migraine with auraS Soriani, C Borgna-Pignatti, E Trabetti, et al.
Molecular and Cellular Probes|June 1, 1995
Allele and genotype frequencies of eight DNA polymorphisms in the Italian populationE Trabetti, R Galavotti, A Casartelli, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 1, 1997
Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndromeA E Turco, E Bresin, S Rossetti, et al.
American Journal of Medical Genetics|August 22, 1997
Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variabilityF Zolezzi, M Valli, M Clementi, et al.
Human Heredity|February 25, 2000
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of italian families with Marfan syndromeM Mottes, S Mirandola, F Rigatelli, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|July 18, 2002
CFTR and cationic trypsinogen mutations in idiopathic pancreatitis and neonatal hypertrypsinemiaM Gomez Lira, C Patuzzo, C Castellani, et al.
Chest|May 16, 2000
Tumor necrosis factor gene complex in COPD and disseminated bronchiectasisC Patuzzo, L S Gilè, M Zorzetto, et al.
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