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Clinical Chemistry and Laboratory Medicine|May 9, 2001
Candidate gene polymorphisms in cardiovascular disease: a comparative study of frequencies between a French and an Italian populationC Pallaud, C Stranieri, C Sass, et al.
Cancer|July 15, 1993
Combined treatment with buserelin and cyproterone acetate in metastatic male breast cancerM Lopez, M Natali, L Di Lauro, et al.
Molecular and Cellular Probes|June 1, 1995
Comparison of heteroduplex and single-strand conformation analyses, followed by ethidium fluorescence visualization, for the detection of mutations in four human genesS Rossetti, S Corrà, M O Biasi, et al.
American Journal of Respiratory and Critical Care Medicine|May 1, 1996
Affected sib-pair and mutation analyses of the high affinity IgE receptor beta chain locus in Italian families with atopic asthmatic childrenL C Martinati, E Trabetti, A Casartelli, et al.
Prenatal Diagnosis|June 1, 1992
Prenatal diagnosis of autosomal dominant polycystic kidney disease using flanking DNA markers and the polymerase chain reactionA Turco, B Peissel, P Quaia, et al.
Bone Marrow Transplantation|December 1, 1989
Bone marrow transplantation monitoring by DNA analysisP Gasparini, G Martinelli, E Trabetti, et al.
Journal of Medical Genetics|August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung diseaseP Gasparini, G Borgo, G Mastella, et al.
Matrix (Stuttgart, Germany)|March 1, 1990
Anomalous cysteine in type I collagen. Localisation by chemical cleavage of the protein using 2-nitro-5-thiocyanobenzoic acid and by mismatch analysis of cDNA heteroduplexesR Tenni, A Rossi, M Valli, et al.
Human Genetics|September 1, 1990
Polymorphic DNA haplotypes and delta F508 deletion in 212 Italian CF familiesG Novelli, P Gasparini, A Savoia, et al.
European Journal of Pediatrics|December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort studyG Borgo, P Gasparini, A Bonizzato, et al.
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