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P FORTINA

Showing results (31-40 of 67) with videos related to

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Hemoglobin|March 1, 1997
alpha-thalassemia caused by a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene including the first nucleotide of the poly A signal sequenceH Tamary, G Klinger, L Shalmon, et al.
Journal of Medical Genetics|July 1, 1994
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigelsA Iolascon, T Parrella, S Perrotta, et al.
Clinical Chemistry|May 1, 1997
Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresisP Fortina, J Cheng, M A Shoffner, et al.
American Journal of Human Genetics|August 1, 1994
Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studiesN B Spinner, E B Rand, P Fortina, et al.
Molecular and Cellular Probes|August 1, 1992
Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the delta F508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) geneP Fortina, R Conant, T Parrella, et al.
British Journal of Haematology|August 1, 1991
A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian familyP Fortina, I Dianzani, A Serra, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 13, 2001
DOP-PCR amplification of whole genomic DNA and microchip-based capillary electrophoresisP Fortina, J Cheng, L J Kricka, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
RFLPs of the phenylalanine hydroxylase gene in the Italian populationI Dianzani, L Farinasso, P Fortina, et al.
PCR Methods and Applications|November 1, 1992
Detection of the most common mutations causing beta-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS)P Fortina, G Dotti, R Conant, et al.
Clinical Genetics|July 18, 2002
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing lossL Bason, T Dudley, K Lewis, et al.
Pageof 7

Showing results (31-40 of 67) with videos related to

Sort By:
Pageof 7
Hemoglobin|March 1, 1997
alpha-thalassemia caused by a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene including the first nucleotide of the poly A signal sequenceH Tamary, G Klinger, L Shalmon, et al.
Journal of Medical Genetics|July 1, 1994
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigelsA Iolascon, T Parrella, S Perrotta, et al.
Clinical Chemistry|May 1, 1997
Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresisP Fortina, J Cheng, M A Shoffner, et al.
American Journal of Human Genetics|August 1, 1994
Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studiesN B Spinner, E B Rand, P Fortina, et al.
Molecular and Cellular Probes|August 1, 1992
Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the delta F508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) geneP Fortina, R Conant, T Parrella, et al.
British Journal of Haematology|August 1, 1991
A newly-characterized alpha-thalassaemia-1 deletion removes the entire alpha-like globin gene cluster in an Italian familyP Fortina, I Dianzani, A Serra, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 13, 2001
DOP-PCR amplification of whole genomic DNA and microchip-based capillary electrophoresisP Fortina, J Cheng, L J Kricka, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
RFLPs of the phenylalanine hydroxylase gene in the Italian populationI Dianzani, L Farinasso, P Fortina, et al.
PCR Methods and Applications|November 1, 1992
Detection of the most common mutations causing beta-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS)P Fortina, G Dotti, R Conant, et al.
Clinical Genetics|July 18, 2002
Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing lossL Bason, T Dudley, K Lewis, et al.
Pageof 7