A Turco|P F Pignatti - JoVE Visualize

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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.

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.

Expert Review of Medical Devices|May 6, 2011

The Integrity bare-metal stent made by continuous sinusoid technologyMark A Turco

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.

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.

Pageof 18

Showing results (21-30 of 180) with videos related to

Sort By:

Pageof 18

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.

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.

Expert Review of Medical Devices|May 6, 2011

The Integrity bare-metal stent made by continuous sinusoid technologyMark A Turco

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.

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.

Pageof 18