Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Camaschella

Showing results (41-50 of 141) with videos related to

Pageof 15
Sort By:
Human Mutation|November 26, 1999
Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, ItalyI Dianzani, U Landegren, C Camaschella, et al.
Haematologica|January 12, 2000
G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosusP Sivera, S Bosio, M T Bertero, et al.
British Journal of Haematology|April 1, 1992
Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFHE Gottardi, M Losekoot, R Fodde, et al.
British Journal of Haematology|May 1, 1976
Clinical and haematological data in 254 cases of beta-thalassaemia trait in ItalyU Mazza, G Saglio, F C Cappio, et al.
Haematologica|March 26, 1999
Variation in the phenotypic expression of C282Y hemochromatosis in an Italian familyS Bosio, G Zecchina, M Cicilano, et al.
American Journal of Human Genetics|March 1, 1991
Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, 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.
Blood Cells, Molecules & Diseases|January 10, 2002
Linkage to chromosome 1q in Greek families with juvenile hemochromatosisG Papanikolaou, M Politou, A Roetto, et al.
Haematologica|November 1, 1990
Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic originA Alfarano, E Gottardi, A Serra, et al.
Genomics|September 1, 1991
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatchI Dianzani, C Camaschella, G Saglio, et al.
Pageof 15

Showing results (41-50 of 141) with videos related to

Sort By:
Pageof 15
Human Mutation|November 26, 1999
Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, ItalyI Dianzani, U Landegren, C Camaschella, et al.
Haematologica|January 12, 2000
G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosusP Sivera, S Bosio, M T Bertero, et al.
British Journal of Haematology|April 1, 1992
Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFHE Gottardi, M Losekoot, R Fodde, et al.
British Journal of Haematology|May 1, 1976
Clinical and haematological data in 254 cases of beta-thalassaemia trait in ItalyU Mazza, G Saglio, F C Cappio, et al.
Haematologica|March 26, 1999
Variation in the phenotypic expression of C282Y hemochromatosis in an Italian familyS Bosio, G Zecchina, M Cicilano, et al.
American Journal of Human Genetics|March 1, 1991
Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, 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.
Blood Cells, Molecules & Diseases|January 10, 2002
Linkage to chromosome 1q in Greek families with juvenile hemochromatosisG Papanikolaou, M Politou, A Roetto, et al.
Haematologica|November 1, 1990
Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic originA Alfarano, E Gottardi, A Serra, et al.
Genomics|September 1, 1991
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatchI Dianzani, C Camaschella, G Saglio, et al.
Pageof 15