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P Gasparini

Showing results (81-90 of 204) with videos related to

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Molecular and Cellular Probes|October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysisC Camaschella, A Roetto, G De Sandre, et al.
Clinical Genetics|July 1, 1997
Detection of dystrophin deletion carriers using FISH analysisS Calvano, E Memeo, M R Piemontese, et al.
Minerva Gastroenterologica E Dietologica|December 9, 2010
Capsule endoscopy of the small bowel in the clinical practice: outpatient management is feasible and cheaperM Soncini, A Russo, E Campi, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patientF M Santorelli, E Bertini, V Petruzzella, et al.
Journal of Chromatography. A|November 22, 1997
Rapid sizing of polymorphic microsatellite markers by capillary array electrophoresisE S Mansfield, M Vainer, D W Harris, et al.
Annals of Neurology|February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentationV Tiranti, L D'Agruma, D Pareyson, et al.
Molecular and Cellular Probes|December 1, 1996
Two polymorphic repeats in the candidate region for the haemochromatosis geneA Grifa, A Totaro, M Carella, et al.
Dermatology (Basel, Switzerland)|October 26, 2012
Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysisF Faletra, I Berti, A Tommasini, et al.
Blood Cells, Molecules & Diseases|August 22, 2000
Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21A Roetto, F Alberti, F Daraio, et al.
Bone Marrow Transplantation|January 1, 1991
An assessment of chimeric transcript detection in CML patients after bone marrow transplantationG Martinelli, M Sessarego, P Gasparini, et al.
Pageof 21

Showing results (81-90 of 204) with videos related to

Sort By:
Pageof 21
Molecular and Cellular Probes|October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysisC Camaschella, A Roetto, G De Sandre, et al.
Clinical Genetics|July 1, 1997
Detection of dystrophin deletion carriers using FISH analysisS Calvano, E Memeo, M R Piemontese, et al.
Minerva Gastroenterologica E Dietologica|December 9, 2010
Capsule endoscopy of the small bowel in the clinical practice: outpatient management is feasible and cheaperM Soncini, A Russo, E Campi, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patientF M Santorelli, E Bertini, V Petruzzella, et al.
Journal of Chromatography. A|November 22, 1997
Rapid sizing of polymorphic microsatellite markers by capillary array electrophoresisE S Mansfield, M Vainer, D W Harris, et al.
Annals of Neurology|February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentationV Tiranti, L D'Agruma, D Pareyson, et al.
Molecular and Cellular Probes|December 1, 1996
Two polymorphic repeats in the candidate region for the haemochromatosis geneA Grifa, A Totaro, M Carella, et al.
Dermatology (Basel, Switzerland)|October 26, 2012
Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysisF Faletra, I Berti, A Tommasini, et al.
Blood Cells, Molecules & Diseases|August 22, 2000
Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21A Roetto, F Alberti, F Daraio, et al.
Bone Marrow Transplantation|January 1, 1991
An assessment of chimeric transcript detection in CML patients after bone marrow transplantationG Martinelli, M Sessarego, P Gasparini, et al.
Pageof 21