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American Journal of Medical Genetics|February 1, 1992
Baller-Gerold syndrome: case report and clinical and radiological reviewB Dallapiccola, L Zelante, R Mingarelli, et al.Neuromuscular Disorders : NMD|March 1, 1995
Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeatsG Novelli, M Gennarelli, E Menegazzo, et al.Human Genetics|January 1, 1979
Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12)B Dallapiccola, L Chessa, P Vignetti, et al.Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 4, 1998
A single polymerase chain reaction-based protocol for detecting normal and expanded alleles in myotonic dystrophyM Gennarelli, M Pavoni, P Amicucci, et al.Human Genetics|January 1, 1983
Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotesB Porfirio, B Dallapiccola, V Mokini, et al.The Journal of Laboratory and Clinical Medicine|August 1, 1988
Protocol for prenatal diagnosis of cystic fibrosis based on studies of alkaline phosphatase isoenzymesG Novelli, F Mannello, C Pierotti, et al.Clinical Genetics|December 1, 1992
Genotyping of spinal muscular atrophy families with linked DNA probesM Gennarelli, S Melchionda, C Fattorini, et al.Acta Haematologica|January 1, 1984
Red blood cell hexokinase in Fanconi's anemiaM Magnani, G Novelli, V Stocchi, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1993
Plasmid DNA and low-frequency electromagnetic fieldsL D'Agruma, A Colosimo, U Angeloni, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1991
Study of the effects on DNA of electromagnetic fields using clamped homogeneous electric field gel electrophoresisG Novelli, M Gennarelli, L Potenza, et al.Pageof 34