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P Gasparini

Showing results (21-30 of 204) with videos related to

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Minerva Medica|December 18, 1998
[Diagnosis of hereditary hemochromatosis with molecular analysis of DNA in patients with anti-HCV positive liver cirrhosis. Clinical case]A M Carella, G Bianco, M Carella, et al.
American Journal of Human Genetics|January 1, 1988
Undergraduate and postgraduate training programs for cytogenetic technologistsR P Gasparini, B J Kaplan, L R Stevens
American Journal of Medical Genetics|May 1, 1991
Sweat chloride concentration in cystic fibrosis patients varies with KM.19 genotype but not with the presence of the common F508 deletionP Gasparini, P F Pignatti, G Borgo, et al.
Molecular and Cellular Probes|February 1, 1992
Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutationsP Gasparini, A Bonizzato, M Dognini, et al.
Clinical Dysmorphology|May 13, 1999
Confirmation of Kapur-Toriello syndrome in an Italian patientL Zelante, M A Candela, A Savoia, et al.
Minerva Cardioangiologica|February 24, 2001
Prognostic significance of markers of thrombin generation in the acute and chronic phases of non cardioembolic ischemic strokeM Soncini, P Gasparini, M Lorena, et al.
Giornale Di Clinica Medica|March 1, 1989
[Juvenile myocardial infarct. A description of 2 cases occurring before 20 years of age and a review of the literature]F Guzzini, L Banfi, R Baroffio, et al.
Panminerva Medica|September 6, 2006
Exclusion of chromosome region 22q12.1-q12.3 as a second locus for Costello syndromeM Bertelli, S Cecchin, A Fabbri, et al.
Annales De Genetique|January 1, 1997
Assignment of ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridizationP Gasparini, S Calvano, E Memeo, et al.
Clinical Dysmorphology|August 24, 2000
A new case of acromegaloid facial appearance (AFA) syndrome with an expanded phenotypeL Zelante, P Gasparini, A Savoia, et al.
Pageof 21

Showing results (21-30 of 204) with videos related to

Sort By:
Pageof 21
Minerva Medica|December 18, 1998
[Diagnosis of hereditary hemochromatosis with molecular analysis of DNA in patients with anti-HCV positive liver cirrhosis. Clinical case]A M Carella, G Bianco, M Carella, et al.
American Journal of Human Genetics|January 1, 1988
Undergraduate and postgraduate training programs for cytogenetic technologistsR P Gasparini, B J Kaplan, L R Stevens
American Journal of Medical Genetics|May 1, 1991
Sweat chloride concentration in cystic fibrosis patients varies with KM.19 genotype but not with the presence of the common F508 deletionP Gasparini, P F Pignatti, G Borgo, et al.
Molecular and Cellular Probes|February 1, 1992
Restriction site generating-polymerase chain reaction (RG-PCR) for the probeless detection of hidden genetic variation: application to the study of some common cystic fibrosis mutationsP Gasparini, A Bonizzato, M Dognini, et al.
Clinical Dysmorphology|May 13, 1999
Confirmation of Kapur-Toriello syndrome in an Italian patientL Zelante, M A Candela, A Savoia, et al.
Minerva Cardioangiologica|February 24, 2001
Prognostic significance of markers of thrombin generation in the acute and chronic phases of non cardioembolic ischemic strokeM Soncini, P Gasparini, M Lorena, et al.
Giornale Di Clinica Medica|March 1, 1989
[Juvenile myocardial infarct. A description of 2 cases occurring before 20 years of age and a review of the literature]F Guzzini, L Banfi, R Baroffio, et al.
Panminerva Medica|September 6, 2006
Exclusion of chromosome region 22q12.1-q12.3 as a second locus for Costello syndromeM Bertelli, S Cecchin, A Fabbri, et al.
Annales De Genetique|January 1, 1997
Assignment of ferritin L gene (FTL) to human chromosome band 19q13.3 by in situ hybridizationP Gasparini, S Calvano, E Memeo, et al.
Clinical Dysmorphology|August 24, 2000
A new case of acromegaloid facial appearance (AFA) syndrome with an expanded phenotypeL Zelante, P Gasparini, A Savoia, et al.
Pageof 21