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P Gasparini

Showing results (71-80 of 204) with videos related to

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Blood|September 25, 1998
Genetic heterogeneity of congenital dyserythropoietic anemia type IIA Iolascon, D De Mattia, S Perrotta, et al.
Molecular and Cellular Probes|August 1, 1997
A frequent polymorphism in the 5' region of the BCMA geneA Roetto, M Cicilano, E Gottardi, et al.
European Journal of Medical Genetics|December 22, 2011
De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short statureM D Perrone, M S Rocca, I Bruno, et al.
Recenti Progressi in Medicina|January 1, 1990
Search of HIV DNA by polymerase chain reaction in the urine sediments of seropositive individualsP Gasparini, A Savoia, P F Pignatti, et al.
American Journal of Human Genetics|November 1, 1994
Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR geneN Morral, R Llevadot, T Casals, et al.
Molecular and Cellular Probes|June 1, 1995
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria modelS Giannattasio, L Bisceglia, P Lattanzio, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Human Genetics|December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndromeP Gasparini, A Grifa, S Savasta, et al.
International Journal of Pediatric Otorhinolaryngology|October 19, 2004
Guidelines and recommendations for testing of Cx26 mutations and interpretation of resultsM Mazzoli, V Newton, A Murgia, et al.
Blood|December 1, 1995
Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")D Girelli, R Corrocher, L Bisceglia, et al.
Pageof 21

Showing results (71-80 of 204) with videos related to

Sort By:
Pageof 21
Blood|September 25, 1998
Genetic heterogeneity of congenital dyserythropoietic anemia type IIA Iolascon, D De Mattia, S Perrotta, et al.
Molecular and Cellular Probes|August 1, 1997
A frequent polymorphism in the 5' region of the BCMA geneA Roetto, M Cicilano, E Gottardi, et al.
European Journal of Medical Genetics|December 22, 2011
De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short statureM D Perrone, M S Rocca, I Bruno, et al.
Recenti Progressi in Medicina|January 1, 1990
Search of HIV DNA by polymerase chain reaction in the urine sediments of seropositive individualsP Gasparini, A Savoia, P F Pignatti, et al.
American Journal of Human Genetics|November 1, 1994
Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR geneN Morral, R Llevadot, T Casals, et al.
Molecular and Cellular Probes|June 1, 1995
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria modelS Giannattasio, L Bisceglia, P Lattanzio, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Human Genetics|December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndromeP Gasparini, A Grifa, S Savasta, et al.
International Journal of Pediatric Otorhinolaryngology|October 19, 2004
Guidelines and recommendations for testing of Cx26 mutations and interpretation of resultsM Mazzoli, V Newton, A Murgia, et al.
Blood|December 1, 1995
Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")D Girelli, R Corrocher, L Bisceglia, et al.
Pageof 21