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ESMO Open|May 20, 2026
Trends in EU regulatory assessment of oncology medicinesT Pabsch, F Pignatti, F Day, et al.
Molecular and Cellular Probes|June 1, 1996
Intrafamilial variable expressivity of osteogenesis imperfecta due to mosaicism for a lethal G382R substitution in the COL1A1 geneL Cohen-Solal, F Zolezzi, P F Pignatti, et al.
Clinical Genetics|October 1, 1991
Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian familiesA Turco, B Peissel, L Gammaro, et al.
Human Molecular Genetics|April 1, 1995
Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasisP F Pignatti, C Bombieri, C Marigo, et al.
Prenatal Diagnosis|May 1, 1989
First-trimester prenatal diagnosis of cystic fibrosis using the polymerase chain reaction: report of eight casesP Gasparini, G Novelli, A Savoia, et al.
American Journal of Respiratory Cell and Molecular Biology|March 1, 1990
The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary diseaseP Gasparini, A Savoia, M Luisetti, et al.
Microbiologica|July 1, 1986
Resistance of HSV-1 growth to aphidicolin in two aphidicolin resistant cell linesG Rappazzo, A Grillo, O Biondi, et al.
Human Heredity|January 1, 1990
Frequency distribution of the alleles of several variable number of tandem repeat DNA polymorphisms in the Italian populationP Gasparini, E Trabetti, A Savoia, et al.
Molecular and Cellular Probes|April 1, 1997
Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA)S Rossetti, S Englisch, E Bresin, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1996
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 geneA E Turco, M Clementi, S Rossetti, et al.
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