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P Gasparini

Showing results (61-70 of 204) with videos related to

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Molecular and Cellular Probes|April 1, 1995
Homozygosity for a novel splice site mutation (2790-2 A--->G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descentC Marigo, C Bombieri, L Bisceglia, et al.
Journal of Medical Genetics|November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosisG Borgo, G Mastella, P Gasparini, et al.
Journal of Medical Genetics|August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung diseaseP Gasparini, G Borgo, G Mastella, et al.
Human Genetics|April 1, 1991
A tetranucleotide repeat polymorphism in the cystic fibrosis geneP Gasparini, M Dognini, A Bonizzato, et al.
Blood|September 18, 1997
Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit geneD Girelli, R Corrocher, L Bisceglia, et al.
American Journal of Medical Genetics|April 14, 1997
Goldenhar complex: a further case with uncommon associated anomaliesL Zelante, P Gasparini, A Castriota Scanderbeg, et al.
Human Genetics|April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphismsP Gasparini, L D'Agruma, G Pio de Cillis, et al.
Digestive Diseases and Sciences|April 29, 1998
Polymorphism of motilin gene in patients with Crohn's diseaseV Annese, A Piepoli, A Andriulli, et al.
Blood|November 14, 1997
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)A Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 1, 1985
Circulating thyroglobulin and antithyroglobulin antibodies after fine needle aspiration of thyroid nodulesA Catania, L Cantalamessa, P Gasparini, et al.
Pageof 21

Showing results (61-70 of 204) with videos related to

Sort By:
Pageof 21
Molecular and Cellular Probes|April 1, 1995
Homozygosity for a novel splice site mutation (2790-2 A--->G) preceding exon 15 of the CFTR gene in a cystic fibrosis patient of North-East Italian descentC Marigo, C Bombieri, L Bisceglia, et al.
Journal of Medical Genetics|November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosisG Borgo, G Mastella, P Gasparini, et al.
Journal of Medical Genetics|August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung diseaseP Gasparini, G Borgo, G Mastella, et al.
Human Genetics|April 1, 1991
A tetranucleotide repeat polymorphism in the cystic fibrosis geneP Gasparini, M Dognini, A Bonizzato, et al.
Blood|September 18, 1997
Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit geneD Girelli, R Corrocher, L Bisceglia, et al.
American Journal of Medical Genetics|April 14, 1997
Goldenhar complex: a further case with uncommon associated anomaliesL Zelante, P Gasparini, A Castriota Scanderbeg, et al.
Human Genetics|April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphismsP Gasparini, L D'Agruma, G Pio de Cillis, et al.
Digestive Diseases and Sciences|April 29, 1998
Polymorphism of motilin gene in patients with Crohn's diseaseV Annese, A Piepoli, A Andriulli, et al.
Blood|November 14, 1997
Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)A Iolascon, E Miraglia del Giudice, S Perrotta, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|January 1, 1985
Circulating thyroglobulin and antithyroglobulin antibodies after fine needle aspiration of thyroid nodulesA Catania, L Cantalamessa, P Gasparini, et al.
Pageof 21